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Spondyloepimetaphyseal dysplasia with multiple dislocations
rareA 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.
- Identifiers
- MONDO:0011335 OMIM:603546Orphanet:93360
- 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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