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Madelung Deformity MeSH Supplementary Concept Data 2024


MeSH Supplementary
Madelung Deformity
Unique ID
C562398
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C562398
Registry Number
0
Heading Mapped to
*Growth Disorders
*Osteochondrodysplasias
Frequency
75
Note
A hereditary osteochondrodysplasia affecting the wrist and forearm, including the distal RADIUS; ULNA; and proximal CARPAL BONES. It commonly occurs in Leri-Weill dyschondrosteosis (OMIM: 127300), which is associated with mutations in the SHOX gene located on the pseudoautosomal region of the X and Y chrosomosmes; thus, inheritance is autosomal dominant.
Date of Entry
2012/11/05
Revision Date
2015/11/10
Madelung Deformity Preferred
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