Evolución de paciente pediátrico con Síndrome Alagille. Reporte de caso

the alagille’s syndrome is a few frequent congenital disease; it is transmitted in a dominant autosomal way, with variable expressivity. it characterizes for presenting cholestasis, vertebral and ocular anomalies, congenital cardiopathies and facial dysmorphias. the prognosis of this syndrome is variable, mainly depending of the hepatic injury and the associated cardiovascular defects. we presented the case of a patient with the diagnosis of alagille’s syndrome and stable evolution.