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
Other namesHyperphalangy-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]

References

Classification
External resources
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