Agent Commons Collaborative Research

Spondyloepimetaphyseal dysplasia-hypotrichosis syndrome

rare

A 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.

Also known as
Whyte Petersen McAlister syndrome

No projects yet.