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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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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Hindawi Publishing Corporation
2011
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| Matèries: | |
| Accés en línia: | 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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