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Expanding the Clinical Picture of Simpson-Golabi-Behmel Syndrome

✍ Scribed by Esther L. Young; Robin Wishnow; Michael A. Nigro


Book ID
116824849
Publisher
Elsevier Science
Year
2006
Tongue
English
Weight
173 KB
Volume
34
Category
Article
ISSN
0887-8994

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πŸ“œ SIMILAR VOLUMES


Clinical and molecular aspects of the Si
✍ Neri, Giovanni; Gurrieri, Fiorella; Zanni, Ginevra; Lin, Angela πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 32 KB πŸ‘ 2 views

The Simpson-Golabi-Behmel syndrome (SGBS) is an overgrowth/multiple congenital anomalies/dysplasia syndrome caused by a mutant X-linked gene. The spectrum of its clinical manifestations is broad, varying from very mild forms in carrier females to infantile lethal forms in affected males. A typically

Cardiac anomalies in the Simpson-Golabi-
✍ Lin, Angela E.; Neri, Giovanni; Hughes-Benzie, Rhiannon; Weksberg, Rosanna πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 11 KB πŸ‘ 2 views
The Simpson–Golabi–Behmel syndrome: A cl
✍ F. Gurrieri; M.G. Pomponi; R. Pietrobono; E. Lucci-Cordisco; E. Silvestri; G. St πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons 🌐 English βš– 133 KB

## Abstract The Simpson–Golabi–Behmel syndrome (SGBS) is an overgrowth condition comprising β€œcoarseness” of facial traits, supernumerary nipples, congenital heart defects, polydactyly and fingernail hypoplasia, and an increased risk of neonatal death and later neoplasia. Psychomotor development is