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Premature Birth with Complicated Perinatal Course Delaying Diagnosis of Prader-Willi Syndrome

Prader-Willi syndrome in the newborn is essentially characterized by marked hypotonia, feeding difficulties, hypogonadism, and possible characteristic facial features. However, diagnosis at this age may be particularly difficult, and dysmorphic features may be subtle or absent. Prematurity can furth...

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Autori principali: Ciana, G., Fertz, M. C., Pecile, V., Demarini, S.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Hindawi Publishing Corporation 2011
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3350041/
https://ncbi.nlm.nih.gov/pubmed/22606524
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2011/981941
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