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Prader–Willi syndrome in neonates: twenty cases and review of the literature in Southern China
BACKGROUND: Prader-Willi syndrome is a rare genetic abnormality that can be challenging to diagnose early, but for which early interventions improve prognosis. METHODS: To improve understanding of Prader–Willi syndrome in neonates in Asia, we retrospectively analyzed the clinical records of 20 affec...
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| Publicat a: | BMC Pediatr |
|---|---|
| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4977863/ https://ncbi.nlm.nih.gov/pubmed/27506196 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12887-016-0662-2 |
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