Simpson-Golabi-Behmel Syndrome

Simpson-Golabi-Behmel Syndrome

Simpson-Golabi-Behmel syndrome is a rare X-linked genetic disorder characterised by prenatal and postnatal overgrowth, facial anomalies, and organ malformations. This condition mainly affects males, with symptoms including a prominent forehead, broad nasal bridge, and large tongue. Early diagnosis and appropriate medical management of Simpson-Golabi-Behmel syndrome are crucial for optimising patient outcomes.