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
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Expanding the Clinical Picture of Simpson-Golabi-Behmel Syndrome
β 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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## Abstract The SimpsonβGolabiβBehmel syndrome (SGBS) is an overgrowth condition comprising βcoarsenessβ 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
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