Hyperammonaemic encephalopathy in a teenage girl

Author:

Magalhães Tiago12ORCID,Campos Teresa3,Rodrigues Esmeralda3,Vasconcelos Carla3,Fontoura Manuel12,Vilarinho Laura4,Leão‐Teles Elisa3

Affiliation:

1. Department of Pediatrics São João Hospital Center Porto Portugal

2. Faculty of Medicine of the University of Porto Porto Portugal

3. Reference Center for Inherited Metabolic Disorders – Centro Hospitalar São João Porto Portugal

4. Human Genetics Department National Health Institute – Dr. Ricardo Jorge Porto Portugal

Publisher

Wiley

Subject

Pediatrics, Perinatology and Child Health

Reference7 articles.

1. Urea cycle disorders—update

2. Inborn Metabolic Diseases

3. Consenso para o tratamento nutricional das Doenças do Ciclo da Ureia 3‐Sociedade Portuguesa de Doenças Metabólicas;Rocha JC;Acta Pediatr Port,2009

4. Late-onset ornithine transcarbamylase deficiency: An under recognized cause of metabolic encephalopathy

5. Nonhepatic Hyperammonemic Encephalopathy Due to Undiagnosed Urea Cycle Disorder

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