A lpha-1-antitrypsin (AAT) deficiency is a common genetic cause of liver disease in the pediatric population (1). AAT deficiency is caused by a mutation in the SERine Protease Inhibitor A1 (SERPINA1) gene on chromosome 14q32.1 (2), leading to the intracellular accumulation of a mutant protein and subsequent hepatocellular damage (1). We present a case of a 2-month-old male patient with jaundice diagnosed with a rare variant of AAT deficiency owing to phenotype PI Ã IS.
Bypass ilio-hepático para revascularización de isquemia mesentérica crónica Revascularization of chronic mesenteric ischemia with common iliac to hepatic artery bypass
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