Liver Involvement in Children with Alpha-1 Antitrypsin Deficiency: A Multicenter Study

PURPOSE: Alpha-1 antitrypsin deficiency (A1ATD) in one of the most common genetic causes of liver disease in children. We aimed to analyze the clinical characteristics and outcomes of patients with A1ATD. METHODS: This study included patients with A1ATD from five pediatric hepatology units. Demograp...

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Detalles Bibliográficos
Autores principales: Cakir, Murat, Sag, Elif, Islek, Ali, Baran, Masallah, Tumgor, Gokhan, Aydogdu, Sema
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition 2020
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7073375/
https://www.ncbi.nlm.nih.gov/pubmed/32206627
http://dx.doi.org/10.5223/pghn.2020.23.2.146

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7073375/
https://www.ncbi.nlm.nih.gov/pubmed/32206627
http://dx.doi.org/10.5223/pghn.2020.23.2.146

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