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Craniofaciofrontodigital syndrome

ORPHA:363705· ICD-10 Q87.0

Definition

Craniofaciofrontodigital syndrome is a rare multiple congenital anomalies syndrome characterized by mild intellectual disability, short stature, cardiac anomalies, mild dysmorphic features (macrocephaly, prominent forehead, hypertelorism, exophthalmos), cutis laxa, joint hyperlaxity, wrinkled palms and soles and skeletal anomalies (sella turcica, wide ribs and small vertebral bodies).

Prevalence
<1 / 1 000 000
Inheritance
Unknown
Age of onset
Neonatal