Congenital hepatic fibrosis in a child with Prader-Willi syndrome: a novel association
Prader–Willi syndrome (PWS) is a rare genetic disorder caused by deletion or unexpression of the chromosome 15 (q 11-13). Symptomatologies include hypotonia, hyperphagia, cognitive impairment, and characteristic dysmorphic profile. Here, we report a 4-year-old boy with PWS who presented with complic...
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| Autori principali: | , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
King Faisal Specialist Hospital and Research Centre
2014-01-01
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| Serie: | Annals of Saudi Medicine |
| Accesso online: | https://www.annsaudimed.net/doi/full/10.5144/0256-4947.2014.81 |
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