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. Signs and symptoms The clinical presentation of this condition is consistent with the following (among others): Highly arched eyebrow Joint stiffness Scoliosis Short stature
Diagnosis Genetic Testing.
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.
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