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    Last Updated: 01/09/2026

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    MediFind found 5 doctor with experience in Brachydactyly Type B near Maryland, US. Of these, 3 are Experienced and 2 are Advanced.

    Location
    LocationClose
    5 providers found
      Advanced in Brachydactyly Type B
      Advanced in Brachydactyly Type B
      2401 W Belvedere Ave, 
      Baltimore, MD 
      Languages Spoken:
      English

      Guney Yilmaz is an Orthopedics provider in Baltimore, Maryland. Dr. Yilmaz is rated as an Advanced provider by MediFind in the treatment of Brachydactyly Type B. His top areas of expertise are Multiple Epiphyseal Dysplasia, Collins Pope Syndrome, Brachydactyly Type B, Tenotomy, and Osteotomy.

      Advanced in Brachydactyly Type B
      Orthopedics | Pediatric Orthopedics
      Advanced in Brachydactyly Type B
      Orthopedics | Pediatric Orthopedics

      University Of Maryland Orthopaedic Associates PA

      1 Texas Station Ct, Fl 3, 
      Lutherville Timonium, MD 
      Languages Spoken:
      English
      Accepting New Patients

      Joshua Abzug is an Orthopedics specialist and a Pediatric Orthopedics provider in Lutherville Timonium, Maryland. Dr. Abzug is rated as an Advanced provider by MediFind in the treatment of Brachydactyly Type B. His top areas of expertise are Compartment Syndrome, Accessory Navicular Bone, Brachial Plexopathy, Fasciotomy, and Osteotomy. Dr. Abzug is currently accepting new patients.

      Experienced in Brachydactyly Type B
      Pediatric Orthopedics | Orthopedics
      Experienced in Brachydactyly Type B
      Pediatric Orthopedics | Orthopedics

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

      10803 Falls Road, Pavilion III STE 2100, Pavilion III STE 2100, 
      Lutherville, MD 
      Languages Spoken:
      English

      Erin Honcharuk, M.D., is a pediatric orthopaedic surgeon with training and expertise in a variety of bone and joint injuries, deformities and diseases affecting children, adolescents, and young adults. She specializes in treating children with conditions affecting the lower extremities, including hip dysplasia, joint instability, clubfoot, bone dysplasias and fractures. She is also skilled in limb-lengthening and reconstructive procedures to correct uneven limbs and treat congenital limb differences. Dr. Honcharuk graduated from the Rutgers-Robert Wood Johnson Medical School in New Jersey, where she received a full scholarship. She completed her residency there in orthopaedic surgery, and was awarded the Resident of the Year Award. She then trained as a pediatric orthopaedic fellow at the Texas Scottish Rite Hospital for Children in Dallas, Texas. She did an additional fellowship at the Paley Orthopaedic and Spine Institute in West Palm Beach, Florida, focusing on limb reconstruction and lengthening. Dr. Honcharuk’s research interests include evaluation and treatment of limb length inequality, traumatic injuries, foot deformities and other pediatric conditions. She is a member of the Pediatric Orthopaedic Society of North America, the American Orthopaedic Association, and the Limb Lengthening and Reconstruction Society. When not at work, Dr. Honcharuk enjoys spending time with her husband and their rescue beagle mix, Furiosa. She also enjoys yoga and baking and decorating cakes. Videos Erin Honcharuk, M.D.Pediatric Orthopaedic Surgeon Leg Length Inequality with Dr. Erin Honcharuk Clubfoot in Children with Dr. Erin Honcharuk. Dr. Honcharuk is rated as an Experienced provider by MediFind in the treatment of Brachydactyly Type B. Her top areas of expertise are Blount Disease, Brachydactyly Type A2, Liebenberg Syndrome, Brachydactyly Type C, and Osteotomy.

      Learn about our expert tiers
      Experienced in Brachydactyly Type B
      Medical Genetics
      Experienced in Brachydactyly Type B
      Medical Genetics

      Rubenstein Child Health Building

      Baltimore, MD 
      Languages Spoken:
      English, Spanish

      Dr. Hilary Vernon is a Professor of Genetic Medicine and pediatrics at the Johns Hopkins University School of Medicine. She is also an attending physician at Kennedy Krieger Institute. Hilary Vernon has expertise in treating inborn errors of metabolism and mitochondrial disorders. She is the director of the Mitochondrial Care Center at The Johns Hopkins Hospital and the Barth Syndrome Interdisciplinary Clinic at the Kennedy Krieger Institute. Her research interests include understanding intermediary metabolism in Barth syndrome and in disorders of branch chain amino acid metabolism. Dr. Vernon also co-directs the Department of Genetic Medicine Clinical Trials Unit, and is the principal investigator on multiple clinical trials for rare diseases. Dr. Vernon received her medical degree and doctorate from Rutgers University, New Brunswick, New Jersey. She completed residencies in genetics and pediatrics at The Johns Hopkins University, and a fellowship in clinical laboratory biochemical genetics at The Johns Hopkins University. Dr. Vernon was recognized with the 2010 Francis F. Schwentker Award for Excellence in Research at Johns Hopkins University and the 2011 James B. Sidbury Jr. Fellowship in Biochemical Genetics at Johns Hopkins University. Dr. Vernon is rated as an Experienced provider by MediFind in the treatment of Brachydactyly Type B. Her top areas of expertise are Methylmalonic Acidemia, Propionic Acidemia, Infantile Neutropenia, Progressive External Ophthalmoplegia, and Gastrostomy.

      Experienced in Brachydactyly Type B
      Pediatrics | Medical Genetics
      Experienced in Brachydactyly Type B
      Pediatrics | Medical Genetics

      Rubenstein Child Health Building

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

      Dr. Julie Hoover-Fong is a Professor of Genetic Medicine and Pediatrics and Director of the Greenberg Center for Skeletal Dysplasias at Johns Hopkins University. Dr. Hoover-Fong holds a bachelor’s degree in Human Nutrition from The Ohio State University, where she also completed her medical degree. She received her Ph.D. in the Graduate Training Program in Clinical Investigation at the Johns Hopkins University School of Medicine and Bloomberg School of Public Health. Dr. Hoover-Fong completed a pediatric internship and residency at Washington University in St. Louis and a fellowship in medical genetics at Johns Hopkins University in Baltimore. She joined the Johns Hopkins University faculty in 2002 and progressed to Professor of Genetic Medicine and Pediatrics in 2019. She practices and oversees the clinical operations, research and educational ventures for the patients, families and healthcare providers served by the Greenberg Center. Her clinical team develops and improves diagnostic and treatment guidelines for comprehensive care of patients with all types of bone conditions including dwarfism, orofacial clefting, craniosynostosis and more. Dr. Hoover-Fong also mentors and teaches medical students, residents and genetic medicine trainees. As an active clinical researcher, Dr. Hoover-Fong is the Principal Investigator of multiple global clinical trials for achondroplasia, the first multi-center, investigator-initiated natural history study for achondroplasia, and multiple clinical studies for patients with orofacial clefting, hypophosphatasia and other conditions. She is also a co-investigator on the ELSI and Phenotype Review Committees for the Mendel Project, a whole exome sequencing venture to identify the genetic cause of Mendelian conditions. From an institutional service perspective, Dr. Hoover-Fong serves on the Johns Hopkins Associate Professor Promotions Committee and the Advisory Committee for the Graduate Training Program in Clinical Investigation. She serves on the Medical Advisory Board of the Little People of America, is a member of the Miller-Coulson Academy of Clinical Excellence at Johns Hopkins University and is a charter member of the International Skeletal Dysplasia Management Consortium, publishing best practice guidelines for patients with skeletal dysplasias. Dr. Hoover is rated as an Experienced provider by MediFind in the treatment of Brachydactyly Type B. Her top areas of expertise are Achondroplasia, Rhizomelic Syndrome, Spondyloepimetaphyseal Dysplasia Strudwick Type, Adenoidectomy, and Myringotomy.

      Showing 1-5 of 5

      Last Updated: 01/09/2026

      What is the definition of Brachydactyly Type B?

      Brachydactyly type B (BDB) is a condition characterized by incomplete development (hypoplasia) or absence of the outermost bones of the fingers and toes (distal phalanges) and nails. Additional features may include hypoplasia of the middle phalanges, fusion of the joints (symphalangism), broad thumbs, and webbed fingers (syndactyly). The feet are often less severely affected than the hands. There are 2 types of this condition, designated as type 1 and 2. BDB type 1 is caused by genetic changes in the ROR2 gene. BDB type 2 is caused by genetic changes in the NOG gene. Inheritance of both types is autosomal dominant.

      When should I see a Brachydactyly Type B doctor in Maryland, US?

      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 Brachydactyly Type B doctor in Maryland, US?

      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 Brachydactyly Type B doctors in Maryland, US?

      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 Brachydactyly Type B doctors in Maryland, US?

      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 Brachydactyly Type B doctor in Maryland, US?

      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 Brachydactyly Type B doctor search results page. 

      Why is it important to get a second opinion from a different Brachydactyly Type B 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 Brachydactyly Type B doctor in Maryland, US?

      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 Brachydactyly Type B 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 Brachydactyly Type B 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 Brachydactyly Type B doctors in Maryland, US?

      Look for the filter feature on the left side of the Brachydactyly Type B 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 Brachydactyly Type B doctor that offers video calls?

      Look for the filter feature on the left-side of the Brachydactyly Type B 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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