Immune Alterations in a Patient With Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome: A Case Report

The hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome is a rare autosomal recessive inborn error of the urea cycle caused by mutations in the SLC25A15 gene. Besides the well-known metabolic complications, patients often present intercurrent infections associated with acute hyperammon...

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Detalles Bibliográficos
Autores principales: Silvera-Ruiz, Silene M., Gemperle, Corinne, Peano, Natalia, Olivero, Valentina, Becerra, Adriana, Häberle, Johannes, Gruppi, Adriana, Larovere, Laura E., Motrich, Ruben D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Immunology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9196877/
https://www.ncbi.nlm.nih.gov/pubmed/35711415
http://dx.doi.org/10.3389/fimmu.2022.861516

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9196877/
https://www.ncbi.nlm.nih.gov/pubmed/35711415
http://dx.doi.org/10.3389/fimmu.2022.861516

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