Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Hereditary disease · Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
Jawad syndrome
Jawad syndrome is a rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterized by congenital microcephaly with facial dysmorphism (sloping forehead, prominent nose, mild retrognathia), moderate to severe, non-progressive intellectual disability and symmetrical digital malformations of variable degree, including brachydactyly of the fifth fingers with single flexion crease, clinodactyly, syndactyly, polydactyly and hallux valgus. Congenital anonychia and white café au lait-like spots on the skin of hands and feet are also associated.
This condition has no sub-types.