Opitz G/BBB syndrome

Opitz G/BBB syndrome (OS) is a multiple congenital anomalies disorder characterized by malformations of the midline including hypertelorism, laryngo-tracheo-esophalgeal defects and hypospadias. There are two clinically indistinguishable genetic subtypes of Opitz G/BBB: X-linked Opitz G/BBB syndrome (XLOS), and autosomal dominant Opitz G/BBB syndrome (ADOS).

Also known as: Opitz G syndrome, Opitz G/BBB syndrome, Opitz GBBB syndrome, Opitz syndrome, Opitz-Frias syndrome, Opitz-GBBB syndrome, hypertelorism-oesophageal abnormality-hypospadias syndrome, hypospadias-dysphagia syndrome

0 clinical trials for this condition and its sub-types, 0 tagged with Opitz G/BBB syndrome itself.