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.

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.