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Familial Prader-Willi syndrome with apparently normal chromosomes

✍ Scribed by Lubinsky, Mark ;Zellweger, Hans ;Greenswag, Louise ;Larson, Gary ;Hansmann, Irving ;Ledbetter, David ;Opitz, John M. ;Reynolds, James F.

Publisher
John Wiley and Sons
Year
1987
Tongue
English
Weight
403 KB
Volume
28
Category
Article
ISSN
0148-7299

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Recently, two female patients with supernumerary small marker X chromosome and a Prader-Willi syndrome (PWS)-like phenotype were reported by Tu Β¨mer et al. [1998]. Both patients presented during childhood with obesity that started around the third year of life, mental retardation, small hands and fe