The 20 Best Hereditary Ataxia Doctors Near Me in Baltimore, MD

Find the Top Hereditary Ataxia Experts and Specialists

Last Updated: 04/28/2026

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MediFind found 103 doctor with experience in Hereditary Ataxia near Baltimore, MD. Of these, 87 are Experienced, 11 are Advanced and 5 are Distinguished.

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103 providers found
    Distinguished in Hereditary Ataxia
    Distinguished in Hereditary Ataxia

    Johns Hopkins Health Care & Surgery Center - Green Spring Station, Lutherville

    Lutherville, MD 
    Languages Spoken:
    English
    Offers Telehealth

    Liana Rosenthal, M.D. is an Assistant Professor in the Department of Neurology at Johns Hopkins University School of Medicine in Baltimore, Maryland. Dr. Rosenthal completed medical school at Johns Hopkins with an internship at Johns Hopkins Bayview Medical Center. She completed her neurology residency and movement disorder fellowship at The Johns Hopkins Hospital. Dr. Rosenthal is rated as a Distinguished provider by MediFind in the treatment of Hereditary Ataxia. She is also highly rated in 27 other conditions, according to our data. Her clinical expertise encompasses Movement Disorders, Parkinson's Disease, Olivopontocerebellar Atrophy, and Spinocerebellar Ataxia. Dr. Rosenthal is board certified in American Board Of Psychiatry And Neurology.

    Distinguished in Hereditary Ataxia
    Distinguished in Hereditary Ataxia

    Johns Hopkins Outpatient Center

    601 North Caroline Street, Floor 5, Floor 5, 
    Baltimore, MD 
    Languages Spoken:
    English, Spanish
    Offers Telehealth

    Dr. Ankur Butala specializes in the care of persons with complex neuropsychiatric conditions, including persons with advanced Parkinson Disease or other movement or neurodegenerative disorders. Upon graduating from a selective Physician-Scientist program at Albany Medical College, he joined the University of Massachusetts in an uncommon residency in both Neurology and Psychiatry. Dual-trained neuropsychiatrists such as Dr. Butala have experience with: Parkinson Disease and atypical Parkinsonism, Huntington Disease, Ataxia, Dystonia, early-onset dementia, traumatic brain injury and chronic traumatic encephalopathy, autism spectrum disorders, medication refractory mood and psychotic disorders, epilepsy and functional neurological disorders. In residency, he developed an interest in circuit models of brain function and how non-pharmacological approaches such as Neuromodulation and brain stimulation may be used to address treatment-resistant conditions. Consequently, he joined Johns Hopkins University School of Medicine as a Clinical and Research Fellow from 2015 to 2018, where he developed a skill set including deep brain stimulation, non-invasive brain stimulation (tDCS), and measurement of eye movements. Currently, Dr. Butala's clinical and research interests are in diagnosing and managing persons with advanced Parkinson's Disease, movement disorders, and neuropsychiatric conditions using neuromodulation, cannabinoids, and entheogens. He has ongoing multidisciplinary collaborations with colleagues at the Whiting School of Engineering - Center of Speech & Language Processing in using Machine-Learning Models and Artificial Intelligence to improve the detection and diagnosis of Movement and Neuropsychiatric disorders. LinkedIn https://www.linkedin.com/in/ankurbutalamd Videos Neurology: Junior Faculty Spotlight. Dr. Butala is rated as a Distinguished provider by MediFind in the treatment of Hereditary Ataxia. He is also highly rated in 42 other conditions, according to our data. His clinical expertise encompasses Parkinson's Disease, Corticobasal Degeneration, Movement Disorders, Drug Induced Dyskinesia, and Deep Brain Stimulation. Dr. Butala is board certified in American Board Of Psychiatry And Neurology.

    Distinguished in Hereditary Ataxia
    Neurology
    Distinguished in Hereditary Ataxia
    Neurology

    Johns Hopkins Outpatient Center

    601 North Caroline Street, Floor 5, Floor 5, 
    Baltimore, MD 
    Languages Spoken:
    English
    Offers Telehealth

    As the director of the Johns Hopkins Movement Disorders Division, Dr. Kelly Mills cares for patients who have movement disorders such as Parkinson’s disease, atypical parkinsonism, dystonia, ataxia, tremor and Huntington’s disease. He also evaluates and manages patients needing deep brain stimulation to manage their movement symptoms and provides botulinum toxin treatment for various disorders. In his research, Dr. Mills explores the cognitive dysfunction that can occur in movement disorders such as Parkinson’s disease. He is particularly interested in describing the role of the basal ganglia in cognition, especially in the context of various diseases that can affect this structure. His work focuses on clarifying how certain treatments might impact cognitive and psychiatric problems. For instance, Dr. Mills studies how deep brain stimulation, when used to treat movement symptoms, can impact cognitive function such as attention, memory or impulsivity. Dr. Mills is a Maryland native and a graduate of the University of Maryland School of Medicine, where he developed an interest in neurology and movement disorders. He trained at the University of California, San Francisco, where he completed his neurology residency as well as a clinical and research fellowship in movement disorders, with a particular emphasis on deep brain stimulation to treat Parkinson’s disease, tremor and dystonia. Dr. Mills is rated as a Distinguished provider by MediFind in the treatment of Hereditary Ataxia. He is also highly rated in 19 other conditions, according to our data. His clinical expertise encompasses Movement Disorders, Parkinson's Disease, Essential Tremor, and Drug Induced Dyskinesia.

    Learn about our expert tiers
    Distinguished in Hereditary Ataxia
    Neuromusculoskeletal Medicine
    Distinguished in Hereditary Ataxia
    Neuromusculoskeletal Medicine

    Johns Hopkins Outpatient Center

    Baltimore, MD 
    Languages Spoken:
    English, French, Spanish
    Offers Telehealth

    Dr. Ricardo Roda earned a combined MD/PhD degree from University of Rochester and completed an adult neurology residency, followed by a clinical neuromuscular fellowship at Johns Hopkins University School of Medicine. During residency, Dr. Roda developed a special interest in both auto-immune disorders and genetic disorders. Following residency, he spent three years in neurogenetics branch of National Institute of Neurological Disorders and Stroke (NINDS) working with Dr. Craig Blackstone, focusing on the use of the newer DNA sequencing techniques in genetic diagnosis, and in establishing genotype/phenotype correlations neuromuscular disorders. His current clinical interests include developing testing strategies for undiagnosed genetic disorders and myasthenia gravis. Dr. Roda is rated as a Distinguished provider by MediFind in the treatment of Hereditary Ataxia. He is also highly rated in 22 other conditions, according to our data. His clinical expertise encompasses Spastic Paraplegia Type 7, Hereditary Spastic Paraparesis, Myasthenia Gravis, and Spastic Paraplegia Type 2. Dr. Roda is board certified in American Board Of Psychiatry And Neurology.

    Advanced in Hereditary Ataxia
    Advanced in Hereditary Ataxia

    Johns Hopkins Outpatient Center

    601 North Caroline Street, Floor 5, Floor 5, 
    Baltimore, MD 
    Languages Spoken:
    English, Farsi

    Dr. Kheradmand is an Associate Professor of Neurology and Otolaryngology-Head and Neck Surgery, and specializes in vertigo, dizziness, imbalance, and disorders of eye movements. Dr. Kheradmand's research combines normal human neurophysiology and investigations in patients with disorders such as ocular misalignment, abnormal eye movements, nystagmus, and vestibular dysfunction. A special focus has been on understanding the mechanisms of spatial disorientation, and how their deleterious effects can be ameliorated. This work is translational, with an iterative process between the clinic and the laboratory with the goal of developing more accurate clinical diagnosis and better modes of treatment. Videos Vestibular Neuritis - Angela's Story Recent News Articles and Media Coverage He Got Dizzy and Sick When He Turned His Head. Why? New York Times (Nov. 7, 2025). Dr. Kheradmand is rated as an Advanced provider by MediFind in the treatment of Hereditary Ataxia. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Hereditary Ataxia and Vertigo. Dr. Kheradmand is board certified in American Board Of Psychiatry And Neurology.

    Advanced in Hereditary Ataxia
    Pediatric Neurology | Neurology
    Advanced in Hereditary Ataxia
    Pediatric Neurology | Neurology

    Johns Hopkins Outpatient Center

    601 North Caroline Street, Floor 5, Floor 5, 
    Baltimore, MD 
    Languages Spoken:
    English

    Dr. Barañano earned her M.D. and Ph.D. degrees from the Johns Hopkins University School of Medicine, where she also completed residencies in pediatrics and neurology, along with a fellowship in neurogenetics at the Kennedy Krieger Institute. Dr. Barañano is an Associate Professor of Clinical Neurology. She specializes in the diagnosis and management of rare neurogenetic disorders. She has a particular interest in the genetic control and function of the cerebellum and expertise in childhood-onset and inherited ataxias. She is a member of the multidisciplinary Fetal Management group and is available for prenatal consultations. Dr. Barañano's research includes collaborative efforts with the Johns Hopkins Department of Genetic Medicine and the Division of Neurogenetics at the Kennedy Krieger Institute. Dr. Baranano is rated as an Advanced provider by MediFind in the treatment of Hereditary Ataxia. She is also highly rated in 22 other conditions, according to our data. Her clinical expertise encompasses Hypotonia, Ohdo Syndrome, Say-Barber-Biesecker-Young-Simpson Variant, Focal or Multifocal Malformations in Neuronal Migration, and Spinocerebellar Ataxia Type 3. Dr. Baranano is board certified in American Board Of Psychiatry And Neurology.

    Advanced in Hereditary Ataxia
    Advanced in Hereditary Ataxia

    Johns Hopkins Outpatient Center

    601 North Caroline Street, Floor 5, Floor 5, 
    Baltimore, MD 
    Languages Spoken:
    English, Arabic, French
    Offers Telehealth

    Dr. Moukheiber trained in neurology at Tufts Medical Center and completed his fellowship in movement disorders at Johns Hopkins. His primary interests include using telehealth/teleneurology to help bridge the gap between tertiary care available in well-funded facilities and the dearth of it in significantly underserved and remote areas; especially pertaining to movement disorders in general and ataxia in particular. He has worked with a number of non-government organizations and founded his own entity that provides home health care in the form of advanced nursing, physical therapy and occupational therapy to underserved communities in third world countries, with particular emphasis on neurodegenerative diseases. Dr. Moukheiber is rated as an Advanced provider by MediFind in the treatment of Hereditary Ataxia. He is also highly rated in 22 other conditions, according to our data. His clinical expertise encompasses Stiff Person Syndrome, Movement Disorders, Parkinson's Disease, and Drug Induced Dyskinesia. Dr. Moukheiber is board certified in American Board Of Psychiatry And Neurology.

    Advanced in Hereditary Ataxia
    Neurology
    Advanced in Hereditary Ataxia
    Neurology

    Johns Hopkins Outpatient Center

    601 North Caroline Street, Floor 5, Floor 5, 
    Baltimore, MD 
    Languages Spoken:
    English
    Offers Telehealth

    With fellowship training in neuro-ophthalmology and additional training in neuro-vestibular disorders, Dr. Daniel Gold sees patients with neuro-ophthalmic disorders (affecting vision, eyelids, pupils, or causing nystagmus or double vision) in addition to oto-neurologic disorders (causing dizziness and vertigo). Videos 2018 Best Consulting Physician Award Tele-(Dizzy) Medicine. Dr. Gold is rated as an Advanced provider by MediFind in the treatment of Hereditary Ataxia. He is also highly rated in 12 other conditions, according to our data. His clinical expertise encompasses Vertigo, Benign Paroxysmal Positional Vertigo, Brown Syndrome, and Stiff Person Syndrome. Dr. Gold is board certified in American Board Of Psychiatry And Neurology.

    Distinguished in Hereditary Ataxia
    Distinguished in Hereditary Ataxia

    Office

    16 S Eutaw St Fl 3, 
    Baltimore, MD 
    Languages Spoken:
    English
    Offers Telehealth

    Joseph Savitt is a Neurologist practicing medicine in Baltimore, Maryland. Dr. Savitt is rated as a Distinguished provider by MediFind in the treatment of Hereditary Ataxia. He is also highly rated in 42 other conditions, according to our data. His clinical expertise encompasses Parkinson's Disease, Movement Disorders, Progressive Supranuclear Palsy, Progressive Supranuclear Palsy Atypical, and Gastrostomy.

    Advanced in Hereditary Ataxia
    Internal Medicine
    Advanced in Hereditary Ataxia
    Internal Medicine

    MDVIP - Bel Air, MD

    208 Plumtree Rd Ste C, 
    Bel Air, MD 
    Languages Spoken:
    English
    Accepting New Patients
    Offers Telehealth

    Sinnarajah Raguraj is a primary care provider, practicing in Internal Medicine in Bel Air, Maryland. Dr. Raguraj is rated as an Advanced provider by MediFind in the treatment of Hereditary Ataxia. He is also highly rated in 48 other conditions, according to our data. His clinical expertise encompasses Anemia, Familial Combined Hyperlipidemia, Xanthoma, and Hypertensive Heart Disease. Dr. Raguraj is currently accepting new patients.

    Experienced in Hereditary Ataxia
    Experienced in Hereditary Ataxia

    Johns Hopkins Outpatient Center

    Baltimore, MD 
    Languages Spoken:
    English, Russian, Spanish, Ukrainian

    Dr. Alexander Pantelyat cares for patients with movement disorders such as Parkinson's disease and related syndromes, essential tremor, dystonia, chorea and normal pressure hydrocephalus. He also provides botulinum toxin injections for movement disorders and is involved in deep brain stimulation programming and intraoperative neurophysiological monitoring.His research explores atypical parkinsonian disorders, such as dementia with Lewy bodies, progressive supranuclear palsy, corticobasal syndrome/degeneration and multiple system atrophy; cognitive aspects of movement disorders; and music-based rehabilitation of neurodegenerative diseases.Dr. Pantelyat earned his medical degree from Temple University School of Medicine in Philadelphia, where he was elected a member of the Alpha Omega Alpha Honor Medical Society and received the Matthew T. Moore Prize in Neurology. He completed his residency training in Neurology ​at the University of Pennsylvania in Philadelphia, and a fellowship in movement disorders at the University of Pennsylvania/Philadelphia VA Medical Center. As part of his fellowship, Dr. Pantelyat also completed the Clinical Research Certificate Program at the Center for Clinical Epidemiology and Biostatistics. He is a 2013 American Academy of Neurology Palatucci Advocacy Leader and grant recipient. Dr. Pantelyat is rated as an Experienced provider by MediFind in the treatment of Hereditary Ataxia. He is also highly rated in 39 other conditions, according to our data. His clinical expertise encompasses Progressive Supranuclear Palsy, Progressive Supranuclear Palsy Atypical, Supranuclear Ophthalmoplegia, and Movement Disorders.

    Experienced in Hereditary Ataxia
    Experienced in Hereditary Ataxia

    Johns Hopkins Outpatient Center

    Baltimore, MD 
    Experience:
    10+ years
    Languages Spoken:
    English
    Offers Telehealth

    Neurologist Ashley Paul specializes in movement disorders and also serves as a clinician educator. Dr. Paul has expertise in Parkinson's Disease, atypical parkinsonism, tremors, chorea, dystonia, ataxia, restless leg syndrome, rapid eye movement sleep behavioral disorders, periodic limb movement of sleep and deep brain stimulation. She offers botulinum toxin injections for the treatment of dystonia. Dr. Paul is rated as an Experienced provider by MediFind in the treatment of Hereditary Ataxia. She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses Movement Disorders, Hereditary Ataxia, Parkinson's Disease, and Drug Induced Dyskinesia. Dr. Paul is board certified in American Board Of Psychiatry And Neurology.

    Experienced in Hereditary Ataxia
    Experienced in Hereditary Ataxia

    Johns Hopkins Outpatient Center

    601 North Caroline Street, Floor 5, Floor 5, 
    Baltimore, MD 
    Languages Spoken:
    English
    Offers Telehealth

    Neurologist Scott Newsome specializes in the care of patients with neuroimmunological and neuroinflammatory disorders of the central nervous system. He works within the Division of Neuroimmunology and Neurological Infections at The Johns Hopkins Hospital, and has special interest in evaluating and treating patients with multiple sclerosis, transverse myelitis, neuromyelitis optica and stiff person syndrome. After completing fellowship training, Dr. Newsome joined the Johns Hopkins Multiple Sclerosis and Transverse Myelitis Centers, and he is the director of the Johns Hopkins Neurosciences Consultation and Infusion Center and the Stiff Person Syndrome Center. He is also director of the Johns Hopkins Neuroimmunology and Neurological Infectious Disease Fellowship Program and co-director of the Multiple Sclerosis Experimental Therapeutics Program. Dr. Newsome received his medical degree from the New York College of Osteopathic Medicine, with honors. During his neurology residency, he was awarded the Golden Apple Outstanding Resident Teaching Award, and later was chosen to be chief resident. He subsequently completed a fellowship in neuroimmunology at The Johns Hopkins Hospital with the support of a Sylvia Lawry Physician Fellowship Award from the National Multiple Sclerosis Society. Identifying and testing novel therapies and therapeutic strategies for multiple sclerosis and other neuroimmunological disorders is Dr. Newsome’s main research focus. Other research endeavors include validating the use of new quantitative clinical outcome measures and imaging techniques in multiple sclerosis and identifying risk factors of disease onset and severity, response to treatment and long-term outcomes in neuroimmunological disorders. An adviser for the National Multiple Sclerosis Society and a member of the Miller-Coulson Academy of Clinical Excellence, Dr. Newsome has also served as president of the Consortium of Multiple Sclerosis Centers. Dr. Newsome is rated as an Experienced provider by MediFind in the treatment of Hereditary Ataxia. He is also highly rated in 15 other conditions, according to our data. His clinical expertise encompasses Stiff Person Syndrome, Multiple Sclerosis (MS), Transverse Myelitis, and Relapsing Multiple Sclerosis (RMS). Dr. Newsome is board certified in American Board Of Psychiatry And Neurology.

    Experienced in Hereditary Ataxia
    Neurology
    Experienced in Hereditary Ataxia
    Neurology

    Johns Hopkins Outpatient Center

    601 North Caroline Street, Floor 5, Floor 5, 
    Baltimore, MD 
    Languages Spoken:
    English
    Offers Telehealth

    Dr. Jee Bang cares for patients with disorders of cognition and movement, such as Huntington disease, progressive supranuclear palsy, corticobasal degeneration, multiple system atrophy, dementia with Lewy bodies, frontotemporal dementia, and Alzheimer disease. Dr. Bang is rated as an Experienced provider by MediFind in the treatment of Hereditary Ataxia. She is also highly rated in 7 other conditions, according to our data. Her clinical expertise encompasses Mcleod Neuroacanthocytosis Syndrome, Huntington Disease, Supranuclear Ophthalmoplegia, and Supranuclear Ocular Palsy. Dr. Bang is board certified in American Board Of Psychiatry And Neurology.

    Experienced in Hereditary Ataxia
    Physiatry
    Experienced in Hereditary Ataxia
    Physiatry

    The Johns Hopkins Hospital

    1800 Orleans Street, Meyer 1-163, Meyer 1-163, 
    Baltimore, MD 
    Languages Spoken:
    English
    Offers Telehealth

    Dr. R. Samuel Mayer is an associate professor of physical medicine and rehabilitation at the Johns Hopkins University School of Medicine. His clinical interests include complications of critical illness, spine disorders, pain management, disorders of muscle tone and cancer rehabilitation. Dr. Mayer serves as the director of cancer rehabilitation, director of undergraduate medical education and residency program director for the Department of Physical Medicine and Rehabilitation. He graduated from the honors program in medical education at Northwestern University School of Medicine and completed his residency in physical medicine and rehabilitation at Rush Medical College. He was chair of the Committee on Medical Education for the American Medical Student Association while he was a medical student. After completing his residency, he remained on faculty at Rush Medical College, eventually becoming the residency program director and acting chair of the Department of Physical Medicine and Rehabilitation. He joined the Department of Physical Medicine and Rehabilitation at Johns Hopkins in 2001. Dr. Mayer serves as director of the Medical Student Summer Clinical Experience in Physical Medicine and Rehabilitation for the Association of Academic Physiatrists. He is Editor in Chief of Knowledge NOW, the American Academy of Physical Medicine and Rehabilitation's online encyclopedia of the field. In 2014, he was named Distinguished Clinician by the American Academy of Physical Medicine and Rehabilitation. Dr. Mayer is rated as an Experienced provider by MediFind in the treatment of Hereditary Ataxia. He is also highly rated in 5 other conditions, according to our data. His clinical expertise encompasses Pediatric Low-Grade Glioma (pLGG), Hemiplegia, Miller-Fisher Syndrome, and Guillain-Barre Syndrome. Dr. Mayer is board certified in American Board Of Physical Medicine And Rehabilitation.

    Experienced in Hereditary Ataxia
    Experienced in Hereditary Ataxia

    Johns Hopkins Bayview Medical Center

    Baltimore, MD 
    Languages Spoken:
    English

    Dr. Michael Polydefkis focuses on neuromuscular diseases, particularly peripheral nerve diseases. He has a special interest in diabetic and HIV-associated peripheral neuropathy. His expertise includes nerve conduction studies, electromyography and nerve, skin and muscle biopsy reading. Dr. Michael Polydefkis received his medical degree from The Johns Hopkins University School of Medicine. He then became a Howard Hughes Medical Institute research fellow before returning to Johns Hopkins to complete an internship and residency in internal medicine, residency in neurology and a fellowship in neuromuscular diseases. Dr. Polydefkis is rated as an Experienced provider by MediFind in the treatment of Hereditary Ataxia. He is also highly rated in 17 other conditions, according to our data. His clinical expertise encompasses Transthyretin Amyloidosis, Familial Transthyretin Amyloidosis, Primary Amyloidosis, and Peripheral Neuropathy.

    Experienced in Hereditary Ataxia
    Physiatry | Pediatrics
    Experienced in Hereditary Ataxia
    Physiatry | Pediatrics

    Kennedy Krieger Institute

    707 North Broadway, Floor 222U, Floor 222U, 
    Baltimore, MD 
    Languages Spoken:
    English

    Sarah Korth, M.D. is an instructor at the Johns Hopkins Department of Physical Medicine and Rehabilitation. She serves as an attending physician at The Johns Hopkins Hospital and the Kennedy Krieger Institute. Dr. Korth’s interests include neuroplasticity of the developing brain, maximizing mobility, spasticity management, neurogenic bowel and bladder management, and a whole-person approach to management of children and adults with congenital conditions, including cerebral palsy and spina bifida. Dr. Korth’s rehabilitation-focused care aims to help people with congenital and acquired disabilities reach their maximum function. Dr. Korth also has an ongoing interest in methods of decreasing health disparities in developing countries. While in medical school, Dr. Korth initiated and developed a sustainable-changes health program called The Paraiso Project in rural Dominican Republic that she actively continues to direct. Dr. Korth is rated as an Experienced provider by MediFind in the treatment of Hereditary Ataxia. She is also highly rated in 7 other conditions, according to our data. Her clinical expertise encompasses Myelomeningocele, Hydrocele, Cerebral Palsy, and Neurogenic Bowel. Dr. Korth is board certified in American Board Of Physical Medicine And Rehabilitation and American Board Of Pediatrics.

    Experienced in Hereditary Ataxia
    Neurology | Pediatric Neurology
    Experienced in Hereditary Ataxia
    Neurology | Pediatric Neurology

    Johns Hopkins Outpatient Center

    601 North Caroline Street, Floor 5, Floor 5, 
    Baltimore, MD 
    Languages Spoken:
    English

    Dr. Tom Crawford has been a member of the Department of Neurology since 1987. He is co-director of the MDA clinic for Neuromuscular Disorders and Neurologist for the Ataxia Telangiectasia Clinical Center at Johns Hopkins. His practice involves general child neurology with a principal interest in caring for children with neuromuscular, neuromotor, and ataxic disorders. Primary research interests involve the basic science and clinical characterization of two important neurologic disorders that affect children: Spinal Muscular Atrophy and Ataxia Telangiectasia. He is also actively involved in the Biology of neurofilaments by characterization of transgenic animal models. He is on the Medical and Scientific Advisory Boards of Families of Spinal Muscular Atrophy, and the Medical Advisory Committee for the Muscular Dystrophy Association. He is the Neurologist for the Ataxia Telangiectasia Clinical Center at Johns Hopkins, which has evaluated almost half of the known patients with this disorder in the United States. Additional specific clinical interests include evaluation and treatment of children with brachial plexus palsies. Dr. Crawford received his medical degree from the University of Southern California. He completed a pediatric internship and residency at the Pediatric Pavilion of the Los Angeles County / University of Southern California Medical Center, followed by a pediatric chief residency. He completed his training in Neurology with Special Qualification in Child Neurology at the Los Angeles Childrens Hospital. He then traveled east to the laboratory of Dr John Griffin at Johns Hopkins for a fellowship in Neuromuscular Disorders. Prior to medical training and Neurology residency, he majored in Psychology and Religion at Yale College. Dr. Crawford has published extensively and presented nationally and internationally. He has an active role in teaching medical students and residents in neurology. In addition, Dr. Crawford has special interest and experience in EMG studies of children and adults. Dr. Crawford is rated as an Experienced provider by MediFind in the treatment of Hereditary Ataxia. He is also highly rated in 13 other conditions, according to our data. His clinical expertise encompasses Primary Lateral Sclerosis, Spinal Muscular Atrophy (SMA), Ataxia-Telangiectasia, and Spinal Muscular Atrophy Type 2. Dr. Crawford is board certified in American Board Of Psychiatry And Neurology and American Board Of Pediatrics.

    Experienced in Hereditary Ataxia
    Medical Genetics | Pediatrics
    Experienced in Hereditary Ataxia
    Medical Genetics | Pediatrics

    Rubenstein Child Health Building

    200 North Wolfe Street, Rubenstein BLDG Lower Level, Rubenstein BLDG Lower Level, 
    Baltimore, MD 
    Languages Spoken:
    English

    Dr. Ada Hamosh is the Dr. Frank V. Sutland Professor of Pediatric Genetics in the Departments of Genetic Medicine and Pediatrics. Since 2002, she has served as clinical director of the McKusick-Nathans Institute of Genetic Medicine, now Department of Genetic Medicine and scientific director of the Online Mendelian Inheritance in Man® (OMIM), a catalog of more than 16,800 human genes and genetic disorders created by Dr. Victor A. McKusick. Her research centers the molecular basis of Mendelian disorders, the integration of genetics into clinical practice and the diagnosis and management of inborn errors of metabolism. Dr. Hamosh earned a bachelor’s degree in biology from Wesleyan University, a medical degree from Georgetown University School of Medicine and a master’s of public health from Johns Hopkins University School of Public Health. She later completed a fellowship in medical and biochemical genetics from the Johns Hopkins School of Medicine, before joining the Johns Hopkins faculty in 1992. Dr. Hamosh began her genetics career focusing on cystic fibrosis, serving as coordinator of the International Cystic Fibrosis Genotype-Phenotype Consortium. She served as chair of the Maryland State Advisory Council for Hereditary & Congenital Disorders from 2001-2009, during which time she also served on the executive committee of the Genetic Counseling Training Program, run by Johns Hopkins University and the National Human Genome Research Institute. Dr. Hamosh has authored more than 128 publications on a variety of topics. In addition, she is a member of 16 professional associations and advisory committees including the American Society of Human Genetics, the Steering Committee of the Global Alliance for Genomics and Health, and the executive board of the Human Genome Organization, of which she will be President from 2023-2025. Dr. Hamosh was recognized in Baltimore magazine as one of the region’s top doctors in 2013, and 2016-2020. Dr. Hamosh is rated as an Experienced provider by MediFind in the treatment of Hereditary Ataxia. She is also highly rated in 28 other conditions, according to our data. Her clinical expertise encompasses Methylmalonic Acidemia, Maple Syrup Urine Disease, Ornithine Transcarbamylase Deficiency, Phenylketonuria (PKU), and Deep Brain Stimulation. Dr. Hamosh is board certified in American Board Of Medical Genetics And Genomics.

    Experienced in Hereditary Ataxia
    Pediatric Orthopedics | Orthopedics
    Experienced in Hereditary Ataxia
    Pediatric Orthopedics | Orthopedics

    Johns Hopkins Outpatient Center

    Baltimore, MD 
    Languages Spoken:
    English, Hindi, Malayalam

    Dr. Ranjit Abraham Varghese is an assistant professor of orthopaedic surgery at the Johns Hopkins University School of Medicine. He is a specialist in pediatric orthopaedics. He focuses on the treatment of cerebral palsy, neuromuscular disorders, andpediatric hip and foot disorders. Dr. Varghese earned his medical degree from Kasturba Medical College of Manipal University in Mangalore India, where he also did his residency. He later earned a master’s degree in health science and clinical epidemiology at the University of British Columbia, Canada. He completed fellowships in pediatric orthopaedics at the University of British Columbia and the University of Minnesota. He also completed a combined orthopedics oncology fellowship at Harvard Medical School, Massachusetts General Hospital, Beth Israel Deaconess Medical Center and Boston Children’s Hospital. He serves as medical director of the Ortho-Cerebral Palsy Program at the Kennedy Krieger Institute. His research interests include cerebral palsy, hip disorders and outcome evaluations. Dr. Varghese is rated as an Experienced provider by MediFind in the treatment of Hereditary Ataxia. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Spastic Diplegia Infantile Type, Slipped Capital Femoral Epiphysis, Wildervanck Syndrome, and CHARGE Syndrome.

    Showing 1-20 of 103

    Last Updated: 04/28/2026

    When should I see a Hereditary Ataxia doctor near Baltimore, MD?

    There are various reasons why you may want to see a specialist, such as: 

    • Your primary care provider recommends it. 
    • Your condition requires expert knowledge and specialized care. 
    • Your symptoms persist or worsen despite treatment. 
    • You need specialized testing or procedures. 
    • You want a second opinion.  

    What should I consider when choosing a Hereditary Ataxia doctor near Baltimore, MD?

    It’s important to see a provider with expertise in your specific condition. Each provider profile in MediFind’s doctor database includes information on which conditions they treat, years of experience, research contributions, languages spoken, insurance plans accepted, and more.  

    How does MediFind rank Hereditary Ataxia doctors near Baltimore, MD?

    MediFind’s rankings are based on a variety of data sources, such as the number of articles a doctor has published in medical journals, participation in clinical trials and industry conferences, as well as the number of patients that provider sees for a given condition. Note that MediFind’s provider database is not based on user reviews, and providers do not pay to be included in the database. 

    What types of insurance are accepted by Hereditary Ataxia doctors near Baltimore, MD?

    Most profiles in MediFind’s doctor database include a list of insurance plans accepted by that provider. However, it’s a good idea to contact the provider’s office to make sure they still accept your insurance, then doublecheck by contacting your insurance plan to confirm they’re in network. 

    How can I book an appointment online with a Hereditary Ataxia doctor near Baltimore, MD?

    MediFind offers direct scheduling for certain providers using the “Request Appointment” button on that provider’s profile. If the schedule option is not available for a provider, tap the red “Show Phone Number” button on their profile to get their contact information. If you prefer to find providers who offer online scheduling, select “Schedules online” under the “Availability” category of the filter feature on the left side of the Hereditary Ataxia doctor search results page. 

    Why is it important to get a second opinion from a different Hereditary Ataxia doctor?

    Second opinions are an opportunity to confirm a diagnosis and its root cause, learn about alternative treatment options, or simply gain peace of mind. Many people, especially those with serious diagnoses, get second opinions so they can understand all their options and make informed decisions, so don’t hesitate to get one if you have any doubts or need more information or clarification regarding your care. Note that some insurance plans require second opinions, while others don’t cover second opinions, so be sure to confirm with your insurance provider first.   

    How can I prepare for my appointment with a Hereditary Ataxia doctor near Baltimore, MD?

    Prepare for your appointment by gathering the following items: 

    • Copies of medical records (dating back at least one year) 
    • Your medical history, including illnesses, medical conditions, surgeries, and other doctors you see 
    • Family history of disease 
    • List of current prescription drugs, over-the-counter medicines, vitamins, and herbal remedies or supplements including names and doses 
    • Allergies to medications, food, latex, insects, etc.  
    • List of questions and concerns 
    • Your insurance card 

    You might also contact the provider’s office to see if they offer transportation or childcare services or if you’re allowed to bring a loved one for support or to take notes during your visit. 

    What questions should I ask my Hereditary Ataxia doctor?

    Here are some sample questions: 

    • Can you explain in simple terms what this condition is and how it’s treated? 
    • What symptoms or side effects should I watch for? 
    • What tests will be involved, and when can I expect results? 
    • Are there other specialists I need to see? 
    • What’s the best way to reach you if I have follow-up questions? 

    How can I learn about the latest clinical trials and research advances my Hereditary Ataxia doctor may know about?

    MediFind’s Clinical Trials tool asks you a series of questions to help you narrow down your search by health condition, age, gender, location, how far you’re willing to travel, and more. Each question you answer filters down the number of trials until you find the ones that are most relevant to you. 

    MediFind’s Latest Advances tool features summaries of recent articles published in medical journals. We use cutting-edge technology to scour medical publication databases for the latest research advancements on any given condition, then we simplify this information in a way that’s useful and easy to understand. 

    Can I filter my search to show male or female Hereditary Ataxia doctors near Baltimore, MD?

    Look for the filter feature on the left side of the Hereditary Ataxia doctor search results page. Select “Female” or “Male” under the “Gender” category to search for female or male providers exclusively. If the “Any” option is selected, it will pull results for both male and female providers. 

    Can I filter my search to find a Hereditary Ataxia doctor that offers video calls?

    Look for the filter feature on the left-side of the Hereditary Ataxia doctor search results page. Select “Offers telehealth visits” under the Availability category to search for providers who offer virtual appointments (video calls). 

    Reviewed on: 11/11/24  

    By: MediFind Medical Staff 

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