Catel–Manzke 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.
Catel–Manzke syndrome | |
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Other names | Hyperphalangy-clinodactyly of index finger with Pierre Robin syndrome |
Prevalence
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]
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Classification | |
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