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A case of classic galactosemia manifesting as neonatal early and profound indirect hyperbilirubinemia
Galactosemia is a rare autosomal recessive metabolic disorder that has three major types. The most common type is classic galactosemia. These patients have deficient galactose-1-phosphate-urydiltransferase. The enzyme deficiency often results in symptomatic disease if breastfeeding or lactose-contai...
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| Publicat a: | Turk Pediatri Ars |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Kare Publishing
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7536454/ https://ncbi.nlm.nih.gov/pubmed/33061763 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.14744/TurkPediatriArs.2019.21298 |
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