The 20 Best Cardiomyopathy Hypogonadism Metabolic Anomalies Doctors Near Me in Maryland, US

Dr. Harry “Hal” Dietz is a professor of pediatrics, an associate professor of medicine and an assistant professor of neurological surgery at the Johns Hopkins University School of Medicine. He is the Victor A. McKusick Professor of Genetics and also serves as the director of the William S. Smilow Center for Marfan Syndrome Research. Recognized as the world’s leading authority on Marfan syndrome, Dr. Dietz conducted genomic mapping and research on therapeutic agents for deficiencies in the genetic protein fibrillin, which is linked to Marfan syndrome. His research contributions have made diagnosis of the condition patient-specific and accurate. He has received more than 50 national and international awards and honors, including the Antoine Marfan Award from the National Marfan Foundation and the Art of Listening Award from the American Heart Association. Dr. Dietz is an ad hoc reviewer for 19 different organizations, including the American Journal of Cardiology, the Archives of Pediatric and Adolescent Medicine, and the Journal of Clinical Investigation. Over more than two decades, Dr. Dietz has mentored 75 predoctoral and postdoctoral researchers. He has authored 282 original publications in peer-reviewed journals, 25 textbook chapters, and 239 abstracts, and has also delivered more than 440 lectures on Marfan syndrome and related genetic disorders. Dr. Dietz completed his B.S. at Duke University and received his M.D. from the SUNY Upstate School of Medicine. He completed a pediatric residency and a cardiology fellowship at Johns Hopkins University before joining the faculty in 1992. Dr. Dietz is rated as an Advanced provider by MediFind in the treatment of Cardiomyopathy Hypogonadism Metabolic Anomalies. He is also highly rated in 81 other conditions, according to our data. His clinical expertise encompasses Manitoba Oculotrichoanal Syndrome, Oculodentodigital Dysplasia, WAGR Syndrome, and CHARGE Syndrome.

Dr. Jaqueline Weissman is an assistant professor in the Department of Neurology, Kennedy Krieger Institute, Department of Pediatrics Johns Hopkins Hospital and Institute of Genomic Medicine at Johns Hopkins Hospital. She is also director of the Center for Tuberous Sclerosis and Related Disorder at Kennedy Krieger Institute. She focuses on genetic and epigenetic causes of neurodevelopmental disorders - particularly intellectual disability - and how specific genetic and epigenetic changes lead to specific neuroanatomic, neurophysiologic and cognitive phenotypes. She is also interested in developing specific cognitive profiles in genetic syndromes as potential outcome measures for trials and to help localize deficits. Currently most of her research is centered around Kabuki Syndrome. Dr. Weissman received her B.A. with. Dr. Harris is rated as an Advanced provider by MediFind in the treatment of Cardiomyopathy Hypogonadism Metabolic Anomalies. She is also highly rated in 89 other conditions, according to our data. Her clinical expertise encompasses Coffin-Lowry Syndrome, Jumping Frenchmen of Maine, Galactosialidosis, and Borjeson-Forssman-Lehmann Syndrome. Dr. Harris is board certified in American Board Of Psychiatry And Neurology.

Inbal Sander is a Dermatologist practicing medicine in Baltimore, Maryland. She has been practicing medicine for over 17 years. Dr. Sander is rated as an Advanced provider by MediFind in the treatment of Cardiomyopathy Hypogonadism Metabolic Anomalies. She is also highly rated in 98 other conditions, according to our data. Her clinical expertise encompasses Warts, Actinic Keratosis, Microcephaly Deafness Syndrome, and Dilated Cardiomyopathy with Hypergonadotropic Hypogonadism.

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 Experienced provider by MediFind in the treatment of Cardiomyopathy Hypogonadism Metabolic Anomalies. 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.

Seiji Ito, MD, is a board certified cardiologist at Children's National. Dr. Ito is rated as an Experienced provider by MediFind in the treatment of Cardiomyopathy Hypogonadism Metabolic Anomalies. He is also highly rated in 12 other conditions, according to our data. His clinical expertise encompasses Tricuspid Atresia, Ebstein's Anomaly, Pulmonary Atresia, Pulmonary Valves Agenesis, and Pacemaker Implantation. Dr. Ito is board certified in Adult Congenital Heart Disease: American Board Of Internal Medicine, 2017, Pediatric Cardiology: American Board Of Pediatrics, 2014, Internal Medicine: American Board Of Internal Medicine, 2011, and Pediatrics: American Board Of Pediatrics, 2011.

Dr. Grant Anhalt is a professor of dermatology at the Johns Hopkins University School of Medicine. His areas of clinical expertise include autoimmune skin diseases and dermatoimmunology. Dr. Anhalt serves as the director of the Dermatoimmunology Laboratory at the Johns Hopkins School of Medicine. He received his undergraduate degree and his M.D. from the University of Manitoba. He completed a residency in internal medicine at the Health Sciences Center in Winnipeg, Canada and a residency in dermatology at the University of Michigan. He performed a fellowship in immunodermatology at the University of Michigan Medical Center. Dr. Anhalt joined the Johns Hopkins faculty in 1982. He was interim chair of the Department of Dermatology from 1996 to 2001. His research interests include autoimmunity, bullous skin diseases and pemphigus and pemphigoid. Dr. Anhalt serves on the medical advisory board for the International Pemphigus & Pemphigoid Foundation. He has been recognized as a top doctor in the Washington Post Magazine, Baltimore Magazine and Castle Connolly Guide. He is a member of several professional organizations, including the American Academy of Dermatology, American Dermatologic Association and American Society for Clinical Investigation. CV http://www.hopkinsmedicine.org/dermatology/our_experts/CV/Anhalt_CV_2014.docx. Dr. Anhalt is rated as an Experienced provider by MediFind in the treatment of Cardiomyopathy Hypogonadism Metabolic Anomalies. He is also highly rated in 24 other conditions, according to our data. His clinical expertise encompasses Pemphigus Vulgaris, Pemphigus, Bullous Pemphigoid, and Pemphigus Foliaceus. Dr. Anhalt is board certified in American Board Of Dermatology.

Eugene Park is a Dermatologist practicing medicine in Baltimore, Maryland. Dr. Park is rated as an Experienced provider by MediFind in the treatment of Cardiomyopathy Hypogonadism Metabolic Anomalies. Her clinical expertise encompasses Van Maldergem Syndrome, Culler Jones Syndrome, Woodhouse-Sakati Syndrome, and DK Phocomelia Syndrome.

Dr. Couser obtained his bachelor’s degree from the University of Virginia and his Medical Doctorate from the Virginia Commonwealth University School of Medicine (VCU SOM). Dr. Couser’s ophthalmology residency was completed at Howard University where he served as co-chief resident in the last year of his residency. He received fellowship training in pediatric ophthalmology and adult strabismus at Emory University. Dr. Couser received a master’s degree in biotechnology from the Johns Hopkins University and completed a residency in clinical genetics at the University of North Carolina at Chapel Hill. He is one of only a few individuals currently board-certified by both the American Board of Ophthalmology and the American Board of Medical Genetics and Genomics. CV https://www.hopkinsmedicine.org/-/media/wilmer/documents/cvs/couser-cv Research Summary My primary research focus involves the identification and management of genetic eye diseases including rare inherited disorders affecting the eyes. Research and scholarly activities have been an integral component of my career path. I have been the principal investigator on 10 clinical trial/IRB studies and a co-investigator on others, participated with several committees or advisory panels related to research activities. I have been credited with over 120 book chapter, journal article and abstract publications. In addition, I served as the primary author/sole editor for a textbook titled Ophthalmic Genetic Diseases: A Quick Reference Guide to the Eye and External Ocular Adnexa Abnormalities, 1st Edition, published by Elsevier in 2018, which is one of only a few textbooks published in this subject area. I also served as a grant review panelist for the National Eye Institute Career Development Awards. Selected Publications *Couser NL, Masood MM, Strande NT, Foreman AKM, Crooks K, Weck KE, Lu M, Wilhelmsen KC, Roche M, Evans JP, Berg JS, Powell CM. 2015. The phenotype of multiple congenital anomalies- hypotonia-seizures syndrome 1: Report and review. Am J Med Genet Part A 9999A:1–6 *Couser NL, Lambert SR. Botulinum toxin: A treatment of consecutive esotropia in children. Strabismus 2012; 20(4):158-161 Couser NL, Lenhart PD, Hutchinson AK. Augmented Hummelsheim procedure to treat complete abducens nerve palsy. J AAPOS 2012;16(4):331-5 *Natario L. Couser, Maheer M. Masood, Arthur S. Aylsworth, and Roger E. Stevenson. Ocular manifestations in the X-linked intellectual disability syndromes. Ophthalmic Genet. 2017, Jan 23:1-12 *Couser NL, Brooks BP, Drack AV, Shankar SP. The evolving role of genetics in ophthalmology. Ophthalmic Genet. 2021 Jan 12:1-4. doi: 10.1080/13816810.2020.1868011. Dr. Couser is rated as an Experienced provider by MediFind in the treatment of Cardiomyopathy Hypogonadism Metabolic Anomalies. He is also highly rated in 13 other conditions, according to our data. His clinical expertise encompasses Epicanthal Folds, Strabismus, Hypotonia, and Brown Syndrome. Dr. Couser is board certified in American Board Of Medical Genetics And Genomics and American Board Of Ophthalmology.

Gerard Martin, MD, FAAP, FACC, FAHA, is a cardiologist at Children's National Hospital, where he has been in practice since 1986. Dr. Martin was promoted to professor of pediatrics (with tenure) at George Washington University School of Medicine & Health Sciences in 1995 and served as the chief of cardiology, 1997-2009, and senior vice president for the Center for Heart, Lung and Kidney Disease, 1999-2015. He founded the Heart and Lung Center in 2004, and was named the 2007 C. Richard Beyda professor of cardiology. Dr. Martin was educated at Syracuse University and the State University of New York, Upstate School of Medicine. After a residency at Brown University and the Rhode Island Hospital, he received training in pediatric cardiology at the Cardiovascular Research Institute at the University of California, San Francisco. He has published over 150 peer-reviewed manuscripts, book chapters, and invited publications and has presented abstracts at over 125 meetings. Dr. Martin is an invited lecturer who has traveled to over 200 meetings, hospitals and universities within the U.S., as well as around the world. Additionally, Dr. Martin is an advocate for congenital heart disease (CHD) efforts nationally and internationally. He played integral roles in the development of CCHD screening and the sub-board of Adult Congenital Heart Disease in the U.S. Dr. Martin also has served as a volunteer on medical missions to developing countries, and as a consultant within the U.S., South America, Asia and the Middle East. Dr. Martin is board-certified in pediatric cardiology, a fellow of the American Academy of Pediatrics and the American College of Cardiology, and a member of the Society for Pediatric Research and the American Board of Pediatrics. He has served or is currently serving on the sub-board of Pediatric Cardiology, American Board of Pediatrics; the chair of the Section Adult Congenital and Pediatric Cardiology, American College of Cardiology; a member of the American Board of Internal Medicine, sub-board of Adult Congenital Heart Disease; and the board of trustees, American College of Cardiology. Dr. Martin is rated as an Experienced provider by MediFind in the treatment of Cardiomyopathy Hypogonadism Metabolic Anomalies. He is also highly rated in 2 other conditions, according to our data. His clinical expertise encompasses Congenital Heart Disease (CHD), Ventricular Septal Defects, Pulmonary Atresia, and Heart Murmurs. Dr. Martin is board certified in Adult Congenital Heart Disease: American Board Of Internal Medicine, 2015, Pediatric Cardiology: American Board Of Pediatrics, 1988, and Pediatrics: American Board Of Pediatrics, 1986.

Dr. Comi graduated from SUNY Buffalo School of Medicine and received her training in pediatrics at the Children's Hospital of Buffalo and her child neurology training at Johns Hopkins Medicine. Her clinical specialization is in the treatment of the neurological aspects of Sturge-Weber syndrome and other disorders related to capillary malformation. Dr. Comi's clinical research interests focus on improving the early diagnosis and treatment of brain involvement in Sturge-Weber syndrome in order to prevent ischemic brain injury in affected infants and young children, and on studies to understand what causes Sturge-Weber syndrome. Her laboratory research work deals with the pathogenesis of Sturge-Weber syndrome, recently shown to be caused by a somatic mutation, and on developing new drug targets, screening assays, models and therapeutic strategies for Sturge-Weber syndrome. Her lab group also works on developing better neuroprotective and neuroregenerative responses to brain injury resulting from impaired blood flow to the brain. Dr. Comi is rated as an Experienced provider by MediFind in the treatment of Cardiomyopathy Hypogonadism Metabolic Anomalies. She is also highly rated in 24 other conditions, according to our data. Her clinical expertise encompasses Sturge-Weber Syndrome, Parkes Weber Syndrome, Stork Bite, Epilepsy in Children, and Endovascular Embolization. Dr. Comi is board certified in American Board Of Psychiatry And Neurology.

Dr. Elrick specializes in the care of children with neuromuscular disorders, and EMG studies in children and adults. He has special interests in genetic neuromuscular and neurodegenerative disorders and Acute Flaccid Myelitis. Dr. Elrick earned his M.D. and Ph.D. in Neuroscience at the University of Michigan Medical School, studying inherited neurodegenerative disorders of childhood. He completed residency training in Pediatrics and Child Neurology, followed by a fellowship in Neuromuscular Medicine and Johns Hopkins before joining the faculty in 2019. Dr. Elrick's laboratory research interest is in understanding mechanisms of neurodegenerative disease, especially those affecting motor neurons. He studies disorders caused by genetic mutations in the nuclear pore complex, the main pathway for transport of material in and out of the nucleus of the cell, including Triple A Syndrome. He also participates in clinical research on Acute Flaccid Myelitis (AFM), aimed at understanding susceptibility to AFM in children, and defining clinical and EMG characteristics of illness and recovery in AFM. Dr. Elrick is rated as an Experienced provider by MediFind in the treatment of Cardiomyopathy Hypogonadism Metabolic Anomalies. He is also highly rated in 2 other conditions, according to our data. His clinical expertise encompasses Cramp-Fasciculation Syndrome, Acute Flaccid Myelitis (AFM), Dysferlinopathy, and Duchenne Muscular Dystrophy. Dr. Elrick is board certified in American Board Of Psychiatry And Neurology.

I am a pediatric neurologist with expertise in epilepsy and electroencephalography (EEG). My clinical and research interests include genetics of epilepsy, medical management of patients with intractable epilepsy and presurgical evaluation of patients who are candidates for epilepsy surgery. Dr. Gupta is rated as an Experienced provider by MediFind in the treatment of Cardiomyopathy Hypogonadism Metabolic Anomalies. He is also highly rated in 7 other conditions, according to our data. His clinical expertise encompasses Benign Rolandic Epilepsy, Lennox-Gastaut Syndrome (LGS), Seizures, and Memory Loss. Dr. Gupta is board certified in American Board Of Psychiatry And Neurology.

Jeffrey A. Becker, MD, is a cardiologist at Children’s National Hospital. In previous roles, he has served as both the Medical Director and Program Director for Outpatient Cardiology. Before joining Children's in 2008, he served as Assistant Chief of Pediatrics and Chief of Pediatric Cardiology at Walter Reed Army Medical Center, retiring as an Army Colonel. Dr. Becker is board certified in general pediatrics and pediatric cardiology, a fellow of the American Academy of Pediatrics and the American College of Cardiology and a member of the North American Society for Cardiac Imaging. He received his doctorate of medicine from the George Washington University School of Medicine, Washington, D.C. He completed his residency in pediatrics at Walter Reed Army Medical Center, Washington, D.C., and his fellowship training in cardiology at Children's National. His primary interests include: non-invasive cardiac imaging and outpatient cardiology. Dr. Becker is rated as an Experienced provider by MediFind in the treatment of Cardiomyopathy Hypogonadism Metabolic Anomalies. He is also highly rated in 3 other conditions, according to our data. His clinical expertise encompasses Sinus of Valsalva Aneurysm, Interrupted Aortic Arch, Patent Ductus Arteriosus, and Ventricular Septal Defects. Dr. Becker is board certified in Pediatric Cardiology: American Board Of Pediatrics, 1998 and Pediatrics: American Board Of Pediatrics, 1991.

Dr. Nara Lygia De Macena Sobreira is an assistant professor at the McKusick-Nathans Department of Genetic Medicine at Johns Hopkins University School of Medicine. Her area of expertise is rare Mendelian phenotypes, analysis of next-generation sequencing, and functional testing of candidate causative variants. She earned her M.D. at the University of Pernambuco in Brazil. She finished her Ph.D. in Human Genetics at Johns Hopkins followed by a one-year postdoc also at Johns Hopkins School of Medicine. During her Ph.D., she worked with Dr. David Valle using next-generation sequencing to elucidate the molecular basis of rare Mendelian phenotypes and in 2010 she discovered PTPN11 as the gene responsible for metachondromatosis by using whole-genome sequencing. She completed residencies in clinical genetics at both Universidade Federal de Sao Paulo and Johns Hopkins. Her main clinical and research focus is on identifying the genetic bases of rare phenotypes, mainly, phenotypes associated with cartilage tumors and vascular anomalies (including Ollier disease and Maffucci syndrome), and on understanding the physiopathology of these phenotypes to identify pharmacological strategies to treat them. She has worked extensively on developing strategies to better analyze the variants identified by next-generation sequencing and on novel strategies for data sharing. She participated on the development of PhenoDB, a phenotypic and genomic database, and created PhenoDB Variant Analysis Tool used worldwide. She is also one of the creators of GeneMatcher, VariantMatcher, and one of the co-founders of the Matchmaker Exchange, all intended to share next-generation sequencing data. She has also worked extensively on functional studies that evaluate the possible pathogenic effects of the candidate causative variants. Recent News Articles and Media Coverage Living the Hopkins Mission Honorees, Johns Hopkins Medicine Successes in Characterizing Genes through GeneMatcher with Nara L. M. Sobreira, MD, PhD, Ambry Genetics (April 30, 2018) Enfermedades raras: el desafio es encontrar otros pacientes que tienen el mismo mal, Lun (26 de septiembre de 2019) 2021 Science Writers' Boot Camp, Johns Hopkins Medicine (June 7, 2021) Making the Perfect Match, Johns Hopkins Medicine (February 1, 2020). Dr. De Macena Sobreira is rated as an Advanced provider by MediFind in the treatment of Cardiomyopathy Hypogonadism Metabolic Anomalies. She is also highly rated in 24 other conditions, according to our data. Her clinical expertise encompasses Spondyloepimetaphyseal Dysplasia Strudwick Type, Greenberg Dysplasia, Blepharophimosis, and Early Infantile Epileptic Encephalopathy. Dr. De Macena Sobreira is board certified in American Board Of Medical Genetics And Genomics.

Edward Primka is a Dermatologist practicing medicine in Leonardtown, Maryland. Dr. Primka is rated as an Experienced provider by MediFind in the treatment of Cardiomyopathy Hypogonadism Metabolic Anomalies. He is also highly rated in 47 other conditions, according to our data. His clinical expertise encompasses Squamous Cell Skin Carcinoma, Basal Cell Skin Cancer, Bowen's Disease, and Liver Spots.

Eric Mallack is a Pediatric Neurologist and a Neurologist practicing medicine in Baltimore, Maryland. Dr. Mallack is rated as an Experienced provider by MediFind in the treatment of Cardiomyopathy Hypogonadism Metabolic Anomalies. He is also highly rated in 4 other conditions, according to our data. His clinical expertise encompasses Adrenoleukodystrophy (ALD), CACH Syndrome, Early Infantile Epileptic Encephalopathy, and Leukodystrophy. Dr. Mallack is board certified in American Board Of Psychiatry And Neurology.

Megan Bone is a Neurologist practicing medicine in Baltimore, Maryland. Dr. Bone is rated as an Experienced provider by MediFind in the treatment of Cardiomyopathy Hypogonadism Metabolic Anomalies. She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses Autism Spectrum Disorder, HNRNPH2-Related Disorder, Distal 18q Deletion Syndrome, and 15q11.2 Microdeletion.

Carol Greene is a Pediatrics provider practicing medicine in Baltimore, Maryland. Dr. Greene is rated as an Experienced provider by MediFind in the treatment of Cardiomyopathy Hypogonadism Metabolic Anomalies. Her clinical expertise encompasses Musculocontractural Ehlers-Danlos Syndrome (mcEDS), Phenylketonuria (PKU), Increased Head Circumference, and MELAS Syndrome. Dr. Greene is board certified in American Board Of Medical Genetics And Genomics and American Board Of Pediatrics.

Dr. Hilary E. Gwynn is an instructor on the medical staff at Kennedy Krieger Institute in the Division of Neurology and Developmental Medicine. She teaches medical trainees and provides patient care at the Center for Development and Learning and on the Pediatric Rehabilitation Unit. She is also the site coordinator for the Johns Hopkins pediatric resident developmental disabilities rotation at the Kennedy Krieger Institute. Dr. Gwynn earned her medical degree at the University of Maryland School of Medicine in Baltimore, Maryland in 2000 and completed her pediatrics residency there in 2003. She subsequently joined the Kennedy Krieger Institute in 2003 to attend the fellowship in neurodevelopmental disabilities through the Kennedy Krieger Institute and Johns Hopkins University School of Medicine. Since graduation from the fellowship program in 2007, she has been an active member of the medical staff at Kennedy Krieger Institute. She teaches medical trainees and provides patient care at the Center for Development and Learning and on the Pediatric Rehabilitation Unit. She is also a member of the clinical staff of the Department of Pediatrics at Johns Hopkins School of Medicine. Contact for Research Inquiries 801 N. Broadway Baltimore, MD 21205 Phone: (443) 923-3246 Research Summary Dr. Gwynn's clinical and research interests include diagnosis and treatment of the child with developmental disability. She is also investigating medical training methodology as it applies to resident and fellow training in the practice of developmental medicine and child neurology. Dr. Gwynn is rated as an Experienced provider by MediFind in the treatment of Cardiomyopathy Hypogonadism Metabolic Anomalies. She is also highly rated in 15 other conditions, according to our data. Her clinical expertise encompasses Cerebral Palsy, Focal Dystonia, Spastic Diplegia Infantile Type, and Moebius Syndrome.

Xiao Zhou is a primary care provider, practicing in Internal Medicine in Rockville, Maryland. Dr. Zhou is rated as an Advanced provider by MediFind in the treatment of Cardiomyopathy Hypogonadism Metabolic Anomalies. He is also highly rated in 82 other conditions, according to our data. His clinical expertise encompasses Alstrom Syndrome, Currarino Triad, Caudal Duplication, and Duane-Radial Ray Syndrome.