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Hepatic vascular malformation in a patient with Simpson–Golabi–Behmel syndrome

✍ Scribed by Elizabeth Cureton; Hua Guo; Olajire Idowu; Sunghoon Kim


Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
226 KB
Volume
143A
Category
Article
ISSN
1552-4825

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Simpson-Golabi-Behmel syndrome (SGBS) is an X-linked overgrowth syndrome caused by deletions in glypican 3 (GPC3). SGBS is characterized by pre- and postnatal overgrowth, a characteristic facial appearance, and a spectrum of congenital malformations which overlaps that of other overgrowth syndromes.