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Catel-Manzke syndrome

rare

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.

Identifiers
MONDO:0014507 OMIM:302380OMIM:616145Orphanet:1388
Causal genes
TGDS
Part of
Multiple congenital anomalies/dysmorphic syndrome-intellectual disabilitySkeletal dysplasia
Also known as
Catel Manzke Syndrome · CATMANS · hyperphalangy-clinodactyly of index finger with Pierre Robin syndrome · index finger anomaly-Pierre Robin syndrome · micrognathia digital syndrome

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