Hyperornithinemia‐hyperammonemia‐homocitrullinuria syndrome in pregnancy: Considerations for management and review of the literature

Hyperornithinemia‐hyperammonemia‐homocitrullinuria (HHH) syndrome is a rare metabolic autosomal recessive urea cycle disorder. Only about 100 patients have been reported in the literature. As the population survives into reproductive years, pregnancy management becomes a new challenge for this clini...

Descripción completa

Detalles Bibliográficos
Autores principales: Ho, Bernice, MacKenzie, Jennifer, Walia, Jagdeep, Geraghty, Michael, Smith, Graeme, Nedvidek, Julie, Guerin, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6498866/
https://www.ncbi.nlm.nih.gov/pubmed/31240152
http://dx.doi.org/10.1002/jmd2.12025

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6498866/
https://www.ncbi.nlm.nih.gov/pubmed/31240152
http://dx.doi.org/10.1002/jmd2.12025

Ejemplares similares