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Up to: Ectodermal dysplasia syndrome

Oculotrichodysplasia

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.

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This condition has no sub-types.