What is another word for simpson-golabi-behmel syndrome?
Pronunciation: [sˈɪmpsənɡˈɒlɐbˌa͡ɪbˈe͡ɪmə͡l sˈɪndɹə͡ʊm] (IPA) 
Simpson-Golabi-Behmel Syndrome is a rare genetic disorder that affects multiple body systems, including the skeletal, cardiac, and nervous systems. This syndrome is also known by other names such as SG Syndrome, Gigantism-Overgrowth Syndrome, and Simpson Dysmorphia Syndrome. The condition is characterized by distinct physical features such as broad forehead, widely spaced eyes, and cleft lip/palate. Patients may also have developmental delays and an increased risk of tumors and organ abnormalities. The disorder can be inherited either in an X-linked recessive or autosomal recessive pattern. Early detection, regular surveillance, and genetic counseling are essential for affected individuals.
