Familial osteodysplasia, Anderson type

Familial osteodysplasia, Anderson type is a rare, genetic dysostosis disorder characterized by craniofacial bone abnormalities (i.e. midface hypoplasia, broad, flat nasal bridge, narrow, thin prognathic mandible with pointed chin, malocclusion, partial dental agenesis) associated with additional osseous anomalies, including scoliosis, calvarial thinning, pointed spinous processes, clinodactyly and abnormal phalanges. Elevated erythrocyte sedimentation rate, hyperuricemia and hypertension have also been reported. There have been no further descriptions in the literature since 1982.

Also known as: osteodysplasia familial Anderson type, osteodysplasia, familial, Anderson type

0 clinical trials for this condition and its sub-types, 0 tagged with Familial osteodysplasia, Anderson type itself.