Sospecha prenatal y diagnóstico postnatal de un paciente con fibrosis quística

Introduction: Cystic fibrosis is a genetic disease of autosomal recessive inheritance, characterized by dysfunction of the exocrine secretion glands.Case report: Male patient 2 years of age, at term (39 weeks). In the third trimester of pregnancy, polyhydramnios, dilated bowel loops and a possible l...

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Bibliographic Details

Published in:	Universidad Médica Pinareña Vol. 15; no. 2; pp. 272 - 278
Main Authors:	Téllez García, Ana Laura, Licourt Otero, Deysi, Toledo Licourt, Melissa
Format:	Journal Article
Language:	Spanish
Published:	2019
Subjects:	Cystic Fibrosis Diseases Enfermedades del Recién Nacido Enfermedades Genéticas Congénitas Fibrosis Quística Genetic Diseases Inborn Infant Newborn
Online Access:	Get full text
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