Early care of N-acetyl glutamate synthase (NAGS) deficiency in three infants from an inbred family

N-acetyl glutamate synthase (NAGS) deficiency is the rarest urea cycle defect presenting as neonatal onset life-threatening hyperammonemia. We report here a family history of severe NAGS deficiency: after the index-case with severe hyperammonemia, one patient benefited from antenatal diagnosis, and...

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Detalles Bibliográficos
Autores principales: Peoc'h, Katell, Damaj, Léna, Pelletier, Romain, Lefèvre, Charles, Dubourg, Christèle, Denis, Marie-Christine, Bendavid, Claude, Odent, Sylvie, Moreau, Caroline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Short Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6994713/
https://www.ncbi.nlm.nih.gov/pubmed/32021803
http://dx.doi.org/10.1016/j.ymgmr.2019.100558

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6994713/
https://www.ncbi.nlm.nih.gov/pubmed/32021803
http://dx.doi.org/10.1016/j.ymgmr.2019.100558

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