Opitz G/BBB syndrome

Disease Overview

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).

Synonyms

• BBB syndrome
• G syndrome
• GBBB syndrome
• Opitz BBBG syndrome
• Opitz G syndrome
• Opitz G/BBB syndrome
• Opitz GBBB syndrome
• Opitz syndrome
• Opitz-Frias syndrome
• Opitz-G syndrome, type 2
• Opitz-GBBB syndrome
• hypertelorism hypospadias syndrome
• hypertelorism with esophageal abnormality and hypospadias
• hypertelorism-oesophageal abnormality-hypospadias syndrome
• hypospadias-dysphagia syndrome
• hypospadias-dysphagia, syndrome
• hypospadias-hypertelorism syndrome
• telecanthus with associated abnormalitiesBBB syndrome
• G syndrome
• GBBB syndrome
• Opitz BBBG syndrome
• Opitz G syndrome
• Opitz G/BBB syndrome
• Opitz GBBB syndrome
• Opitz syndrome
• Opitz-Frias syndrome
• Opitz-G syndrome, type 2
• Opitz-GBBB syndrome
• hypertelorism hypospadias syndrome
• hypertelorism with esophageal abnormality and hypospadias
• hypertelorism-oesophageal abnormality-hypospadias syndrome
• hypospadias-dysphagia syndrome
• hypospadias-dysphagia, syndrome
• hypospadias-hypertelorism syndrome
• telecanthus with associated abnormalities