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Case Report

A Case of Prader-Willi Syndrome with FUO Diagnosed at Infancy

Jun Ho Kim, Jin Hwa Jeong, Sung Min Cho

Clin Exp Pediatr. 2000;43(8):1142-1148. Published online August 15, 2000

Prader-Willi syndrome(PWS) was first described by Prader et al in 1956. This syndrome is characterized by diminished fetal activity, low birth weight, infantile hypotonia with feeding problem, temperature instability, early onset of childhood hyperphagia with consequent obesity, short stature, hypogonadism and mental retardation. The deletion of chromosome 15(del 15(q11-13)) was reported by Ledbetter in 1981, which was thought to be...

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