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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Detalles Bibliográficos
Autores principales: Ciana, G., Fertz, M. C., Pecile, V., Demarini, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3350041/
https://www.ncbi.nlm.nih.gov/pubmed/22606524
http://dx.doi.org/10.1155/2011/981941

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3350041/
https://www.ncbi.nlm.nih.gov/pubmed/22606524
http://dx.doi.org/10.1155/2011/981941

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