Article
Prader-Willi syndrome.
European journal of human genetics : EJHG - 1 Jan 2009
Cassidy Suzanne B, Driscoll Daniel J
Abstract excerpt
Prader-Willi syndrome (PWS) is a highly variable genetic disorder affecting multiple body systems whose most consistent major manifestations include hypotonia with poor suck and poor weight gain in infancy; mild mental retardation, hypogonadism, growth hormone insufficiency causing short stature for the family, early childhood-onset hyperphagia and obesity, characteristic appearance, and behavioral and sometimes...
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