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Spondyloepimetaphyseal dysplasia-hypotrichosis syndrome
rareA rare primary bone dysplasia disorder characterized by congenital hypotrichosis associated with rhizomelic short stature (more pronounced in upper limbs than lower limbs), limited hip abduction and mild genu varum. Flared and irregular metaphyses, delayed and irregular epiphiseal ossification and pear-shaped vertebral bodies are characteristic radiologic findings.
- Identifiers
- MONDO:0008469 OMIM:183849Orphanet:168443
- Part of
- Spondyloepimetaphyseal dysplasia
- Also known as
- Whyte Petersen McAlister syndrome
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