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Early diagnosis and care is achieved but should be improved in infants with Prader-Willi syndrome
BACKGROUND: PWS is a severe neurodevelopmental genetic disorder now usually diagnosed in the neonatal period from hypotonia and feeding difficulties. Our study analyzed the birth incidence and care of infants with early diagnosis. METHODS: Data were collected on 61 infants with a molecular diagnosis...
Gorde:
| Argitaratua izan da: | Orphanet J Rare Dis |
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| Egile Nagusiak: | , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
BioMed Central
2017
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5490212/ https://ncbi.nlm.nih.gov/pubmed/28659150 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-017-0673-6 |
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