Gorlin-Chaudhry-Moss Syndrome

Gorlin-Chaudhry-Moss Syndrome

Gorlin-Chaudhry-Moss syndrome is a rare genetic disorder characterised by craniofacial dysmorphisms, hypertrichosis, and developmental abnormalities. Affecting both males and females, this condition arises from mutations in the SALL1 gene. Management focuses on symptomatic treatment and multidisciplinary support. Gorlin-Chaudhry-Moss syndrome typically requires early and ongoing medical intervention.