PRADER-WILLI SYNDROME - A CASE-REPORT

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作者
AIREDE, KI
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R5 [内科学];
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1002 ; 100201 ;
摘要
A case of a male infant presenting in the neonatal period is described to highlight the morbidity of Prader-Willi. His features included marked hypotonia, feeding difficulty, hypogonadism and typically dysmorphic facies. Marked improvement in muscle tone was noted by 5 months of age. Emphasis is placed on its neonatal presentation and possible aetiologic mechanisms. The natural history is also noted.
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页码:831 / 838
页数:8
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