Evolución de paciente pediátrico con Síndrome Alagille. Reporte de caso Evolution of a pediatric patient with Alagille’s Syndrome. Report of a case

Evolución de paciente pediátrico con Síndrome Alagille. Reporte de caso Evolution of a pediatric patient with Alagille’s Syndrome. Report of a case

El síndrome de Alagille es una enfermedad congénita y poco frecuente, se transmite de forma autosómica dominante, con expresividad variable. Se caracteriza por presentar colestasis, anomalías vertebrales y oculares, cardiopatía congénita y dismorfias faciales. El pronóstico de este síndrome es varia...

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Bibliographic Details
Main Authors:	Estela V Román Castellini, Ibis Umpiérrez García, Félix M Ponce Rodríguez, María de los Ángeles López Zayas
Format:	Article
Language:	English
Published:	Universidad de Ciencias Médicas de Matanzas 2012-04-01
Series:	Revista Médica Electrónica
Subjects:	afectación hepática autosómica dominante defectos cardiovasculares enfermedad congénita niño síndrome de Alagille hepatic damage autosomal dominant cardiovascular defects congenital disease child Alagille’s Syndrome
Online Access:	http://scielo.sld.cu/scielo.php?script=sci_arttext&pid=S1684-18242012000200012

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