Compound heterozygote variants: c.848A > G; p.Glu283Gly and c.890C > T; p.Ala297Val, of Isovaleric acid-CoA dehydrogenase (IVD) gene causing severe Isovaleric acidemia with hyperammonemia

With the execution of expanded newborn screen (NBS) program nationwide, it is uncommon to see severe hyperammonemia associated with isovaleric acidemia (IVA). We present a seven-day-old boy with severe IVA complicated by hyperammonemia. This child was flagged by NBS at 4 days old, but confirmatory t...

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Detalles Bibliográficos
Autores principales: Tsai, Anne Chun-Hui, Lin, Hsin-Ti, Chou, Maxwell, Bolen, Jessica, Zimmerman, Chelsea, DeMarzo, Danielle, Enchautegui-Colon, Yazmin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Short Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9248227/
https://www.ncbi.nlm.nih.gov/pubmed/35782626
http://dx.doi.org/10.1016/j.ymgmr.2022.100859

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9248227/
https://www.ncbi.nlm.nih.gov/pubmed/35782626
http://dx.doi.org/10.1016/j.ymgmr.2022.100859

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