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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...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition
2020
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| Materias: | |
| 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 |