| Literature DB >> 24357529 |
Guillaume Jedraszak1, Muriel Girard, Antonio Mellos, Djamal-Dine Djeddi, Christophe Chardot, Audrey Vanrenterghem, Marie-Pierre Moizard, Jean Gondry, Henri Sevestre, Michele Mathieu-Dramard, Florence Lacaille, Benedicte Demeer.
Abstract
Simpson-Golabi-Behmel syndrome type 1 (SGBS1) -OMIM 312870- is a rare X-linked inherited overgrowth syndrome caused by a loss of function mutation in the GPC3 gene. Affected patients present a variable phenotype with pre- and post-natal macrosomia, distinctive facial dysmorphism, organomegaly, and multiple congenital anomalies. Intellectual disability is not constant. About 10% of patients have an increased risk of developing embryonic tumors in early childhood. Only one case of biliary disease has been described so far. GPC3 is localized on Xq26. It encodes for glypican 3, a heparan sulfate proteoglycan, which among its different known roles, negatively regulates liver regeneration and hepatocyte proliferation. This report concerns a male with a SGBS1, carrier of a GPC3 pathogenic mutation, and neonatal liver disease, who developed an early biliary cirrhosis. Together with the associated risk of cancer and developmental delay, liver transplantation was discussed and then successfully performed at the age of 19 months. A hypothesis on the role of GPC3 in the patient's liver disease is also proposed.Entities:
Keywords: GPC3; Simpson-Golabi-Behmel syndrome; biliary cirrhosis; liver transplantation
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Year: 2013 PMID: 24357529 DOI: 10.1002/ajmg.a.36335
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802