Prader-Willi syndrome | Genetic and Rare Diseases …

January 23, 2021

Prader-Willi syndrome (PWS) is a genetic condition that affects many parts of the body. Infants with PWS have severe hypotonia (low muscle tone), feeding difficulties, and slow growth. In later infancy or early childhood, affected children typically begin to eat excessively and become obese.Other signs and symptoms often include short stature, hypogonadism, developmental delays, cognitive …

https://rarediseases.info.nih.gov/diseases/5575/prader-willi-syndrome

Prader-Willi syndrome | Genetic and Rare Diseases … <body> <h1> Array ( [0] => orader-willi syndrome | genetic and rare diseases … [1] => lrader-willi syndrome | genetic and rare diseases … [2] => -rader-willi syndrome | genetic and rare diseases … [3] => 0rader-willi syndrome | genetic and rare diseases … [4] => peader-willi syndrome | genetic and rare diseases … [5] => pdader-willi syndrome | genetic and rare diseases … [6] => pfader-willi syndrome | genetic and rare diseases … [7] => ptader-willi syndrome | genetic and rare diseases … [8] => p5ader-willi syndrome | genetic and rare diseases … [9] => p4ader-willi syndrome | genetic and rare diseases … [10] => przder-willi syndrome | genetic and rare diseases … [11] => prsder-willi syndrome | genetic and rare diseases … [12] => prwder-willi syndrome | genetic and rare diseases … [13] => prqder-willi syndrome | genetic and rare diseases … [14] => praser-willi syndrome | genetic and rare diseases … [15] => praxer-willi syndrome | 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