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PubMed · 1813307

Prader-Willi syndrome: a case report.

K I Airede
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Abstract

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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HumansInfant, NewbornMaleMotor SkillsMuscle TonusPrader-Willi SyndromeCase ReportsJournal Article

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K I Airede. 1991. Prader-Willi syndrome: a case report.. https://pubmed.ncbi.nlm.nih.gov/1813307/

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