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Up to: Ectodermal dysplasia syndrome
Oculoosteocutaneous syndrome
A syndrome is characterized by congenital anodontia, a small maxilla, short stature with shortened metacarpals and metatarsals, sparse hair, albinoidism and multiple ocular anomalies. It has been described in three siblings (one brother and two sisters). Transmission is autosomal recessive.
This condition has no sub-types.