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Congenital Hypothyroidism: An Unusual Combination of Biochemical Abnormalities
A forty-five-day-old female infant presented with prolonged jaundice with clinical features suggestive of congenital hypothyroidism (CHT). On investigations, the infant was noted to have indirect hyperbilirubinemia (13.8 mg/dl) with increased levels of AST (298 IU/dl) and ALT (174 IU/dl) in the seru...
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| Yayımlandı: | Case Rep Pediatr |
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| Asıl Yazarlar: | , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Hindawi Publishing Corporation
2016
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5138475/ https://ncbi.nlm.nih.gov/pubmed/27994903 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2016/2678578 |
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