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Simpson-Golabi-Behmel syndrome

Congenital Malformations and Chromosomal Abnormalities

Simpson-Golabi-Behmel syndrome, abbreviated SGBS, is a rare inherited congenital disorder that can cause craniofacial, skeletal, vascular, cardiac and renal abnormalities. It carries a notably high prevalence of cancer, including Wilms tumor, neuroblastoma, and tumors of the adrenal gland, liver, lungs and other abdominal organs. It follows an X-linked recessive inheritance pattern: females who carry a single mutated copy are generally considered carriers, though they can still show symptoms ranging from mild to severe, while affected males face an increased risk of fetal death. It is associated with mutations in the GPC3 and OFD1 genes and falls under medical genetics. It is also known by several other names, including Golabi-Rosen syndrome, Simpson dysmorphia syndrome and X-linked dysplasia gigantism syndrome.

Facts
Classification
ICD-10 Chapter
XVII: Congenital Malformations, Deformations and Chromosomal Abnormalities 1
Communicable or Non-communicable
Non-Communicable 2
Causative Agent
Causative Agent (category)
Genetic / Hereditary 2
Sources
1. Wikidata: Simpson-Golabi-Behmel syndrome
Wikidata P494 (Q87.0)View the Source
2. Simpson-Golabi-Behmel syndrome (Wikipedia)
  • infobox causes
    causes: Genetic
  • Lead: disease category
    Simpson-Golabi-Behmel syndrome (SGBS) is a rare inherited congenital disorder that can cause craniofacial, skeletal, vascular, cardiac, and renal abnormalities.
View the Source
Simpson-Golabi-Behmel syndrome (Wikipedia)
Lead section
Quote, Lead section
Simpson-Golabi-Behmel syndrome (SGBS) is a rare inherited congenital disorder that can cause craniofacial, skeletal, vascular, cardiac, and renal abnormalities.
View the Source
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