Catel–Manzke syndrome

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Catel–Manzke syndrome
Other namesHyperphalangy-clinodactyly of index finger with Pierre Robin syndrome

Catel–Manzke syndrome is a rare genetic disorder characterized by distinctive abnormalities of the index fingers; the classic features of Pierre Robin syndrome; occasionally with additional physical findings.

Diagnosis[edit]

Prevalence[edit]

Currently there are only around 26 people in the world that are known to have this rare condition. Inheritance is thought to be X-linked recessive.[1]

References[edit]

External links[edit]

Classification
External resources