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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?
Elite in Chondrodystrophy
Medical Genetics | Pediatrics
Elite in Chondrodystrophy
Medical Genetics | Pediatrics
A.i. Dupont Hospital For Children, 1600 Rockland Road, 
Wilmington, DE 
Languages Spoken:
English
Accepting New Patients

Michael Bober is a Medical Genetics specialist and a Pediatrics provider in Wilmington, Delaware. 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. Dr. Bober is currently accepting new patients.

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?
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.

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Rare Diseases Clinical Research Network Brittle Bone Disease Consortium Longitudinal Study of Osteogenesis Imperfecta

Summary: Osteogenesis Imperfecta (OI) is a rare disorder of increased bone fragility characterized by fractures with minimal or absent trauma, dentinogenesis imperfecta (DI), and, in adult years, hearing loss. It is seen in both genders and all races. The clinical features of OI represent a continuum varying from perinatal lethality to individuals with severe skeletal deformities, mobility impairments, and...