Gastropatía hipertrófica perdedora de proteínas. Enfermedad de Ménétrier. Caso clínico.

Introduction: Ménétrier disease is a rare disorder characterized by gastric foveolar hyperplasia associated with secondary protein loss. In children, this condition is presented as an edematous syndrome without renal or hepatic impairment and differs from the adult form by the constant presence of e...

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Bibliographic Details

Published in:	Revista Chilena de Pediatría Vol. 85; no. 1; pp. 81 - 87
Main Authors:	KIRBERG B., ARTURO, RODRÍGUEZ V., BRINY, DONOSO V., FRANCISCO, KIRHMAN T., MÓNICA, NORIEL V., MARISOL
Format:	Article
Published:	Revista Chilena de Pediatria feb2014
Subjects:	Hypertrophy Protein deficiency Hyperplasia Helicobacter pylori Juvenile diseases
Online Access:	View this record in EBSCOhost