Oculotrichodysplasia

MONDO:0009771

Oculotrichodysplasia is characterized by retinitis pigmentosa, trichodysplasia, dental anomalies, and onychodysplasia. It has been described in two siblings (brother and sister) born to first cousin parents. Transmission appears to be autosomal recessive.

Also known as: Cecato de Lima-Pinheiro syndrome, oculotrichodysplasia, OTD

0 clinical trials for this condition and its sub-types, 0 tagged with Oculotrichodysplasia itself.

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↑ Ectodermal dysplasia syndrome (45)

Including sub-types (0) Tagged with Oculotrichodysplasia (0)

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