Simpson-Golabi-Behmel syndrome
What is Simpson-Golabi-Behmel syndrome?
Simpson-Golabi-Behmel syndrome (SGBS, also referred to as SGBS type 1) is a rare X-linked multiple congenital anomalies syndrome, characterized by pre- and postnatal overgrowth, distinctive craniofacial features, variable congenital malformations, organomegaly and an increased tumor risk.
Other condition names
- DGSX
- Golabi-Rosen syndrome
- SDYS
- SGBS
- SGBS1
- Simpson dysmorphia syndrome
- Simpson-Golabi-Behmel syndrome type 1
- X-linked dysplasia gigantism syndrome
Inheritance type
X-linked recessive
Prevalence
- Worldwide: Unknown
Age of Onset
- Antenatal
- Childhood
- Infancy
- Neonatal
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