Chondrodystrophy
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Learn About Chondrodystrophy

Condition 101 content is not available at this time, but we are continually updating the site. Please check back.

However, there may be experts who have treated this or similar conditions in our Find a Doctor section and research may be available in our Latest Advances section.

Who are the top Chondrodystrophy Local Doctors?
Michael B. Bober
Elite in Chondrodystrophy
Medical Genetics
Elite in Chondrodystrophy
Medical Genetics

Nemours Children's Hospital, Delaware

1600 Rockland Road, 
Wilmington, DE 
Experience:
32+ years
Languages Spoken:
English

Dr. Michael B. Bober is a pediatric geneticist and an authority on skeletal dysplasias, brittle bone disease, primordial dwarfism and other genetic disorders of the skeleton. He is a frequent guest lecturer, accomplished author and consultant for numerous television networks, here and abroad. Dr. Bober is rated as an Elite provider by MediFind in the treatment of Chondrodystrophy. His top areas of expertise are Microcephalic Osteodysplastic Primordial Dwarfism Type 2 (MOPD2), Microcephalic Osteodysplastic Primordial Dwarfism Type 1 (MOPD1), Achondroplasia, Osteotomy, and Adenoidectomy.

Elite in Chondrodystrophy
Elite in Chondrodystrophy
Ankara, TR 

Pelin Kiper-Simsek practices in Ankara, Turkey. Ms. Kiper-Simsek is rated as an Elite expert by MediFind in the treatment of Chondrodystrophy. Her top areas of expertise are Chondrodystrophy, Schwartz-Jampel Syndrome, X-Linked Spondyloepiphyseal Dysplasia Tarda, and Brachydactyly Mononen Type.

 
 
 
 
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Elite in Chondrodystrophy
Elite in Chondrodystrophy
Manipala, KA, IN 

Katta Girisha practices in Manipala, India. Girisha is rated as an Elite expert by MediFind in the treatment of Chondrodystrophy. Their top areas of expertise are Pyle Disease, Brachydactyly Mononen Type, Congenital Contractures, and Arthrogryposis Multiplex Congenita.

What are the latest Chondrodystrophy Clinical Trials?
Longitudinal Study of Neurodegenerative Disorders

Summary: The purpose of this study is to understand the course of rare genetic disorders that affect the brain. This data is being analyzed to gain a better understanding of the progression of the rare neurodegenerative disorders and the effects of interventions.

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Study of the Natural History, Pathogenesis and Outcome of Melorheostosis - a Rare Osteosclerotic Disease

Background: \- The rare disease melorheostosis causes bones to thicken. This may lead to pain, and can affect bones, joints, and muscles. Researchers want to learn more about the disease and how it progresses.