Catel-Manzke syndrome

Catel-Manzke syndrome is a rare bone disease characterized by bilateral hyperphalangy and clinodactyly of the index finger typically in association with Pierre Robin sequence comprising micrognathia, cleft palate and glossoptosis.

Also known as: Catel Manzke Syndrome, Catel-Manzke syndrome, Palatodigital syndrome, Catel-Manzke type, Pierre Robin sequence-hyperphalangy-clinodactyly syndrome, Pierre Robin syndrome-hyperphalangy-clinodactyly syndrome, hyperphalangy-clinodactyly of index finger with Pierre Robin syndrome, index finger anomaly-Pierre Robin syndrome, micrognathia digital syndrome

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