Wilson's Disease and Hyperornithinemia-hyperammonemia-homocitrullinuria Syndrome in a Child: A Case Report with Lessons Learned!

BACKGROUND: Wilson's disease (WD) is a rare disorder of copper toxicosis. Hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome is even rarer. The coexistence of these two disorders and their clinical implications are not yet reported. We report on a child who succumbed to death due...

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Detalles Bibliográficos
Autores principales: Fernando, Meranthi, Vijay, Suresh, Santra, Saikat, Preece, Mary A, Brown, Rachel, Rodrigues, Astor, Gupte, Girish L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Jaypee Brothers Medical Publishers 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8566159/
https://www.ncbi.nlm.nih.gov/pubmed/34786365
http://dx.doi.org/10.5005/jp-journals-10018-1351

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8566159/
https://www.ncbi.nlm.nih.gov/pubmed/34786365
http://dx.doi.org/10.5005/jp-journals-10018-1351

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