Agent Commons Collaborative Research

Spondyloepimetaphyseal dysplasia with multiple dislocations

rare

A rare disorder caused by mutation in the KIF22 gene. It is characterized by short stature, midface retrusion, progressive knee malalignment, generalized ligamentous laxity, and mild spinal deformity.

Causal genes
KIF22
Also known as
SEMD-MD · SEMDJL2 · spondyloepimetaphyseal dysplasia with joint laxicity, Hall type · spondyloepimetaphyseal dysplasia with JOINT laxity type 2 · spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type

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