Progress of the congenital glucose-galactose malabsorption / 国际儿科学杂志
International Journal of Pediatrics
;
(6): 663-666, 2017.
Artigo
em Chinês
| WPRIM
| ID: wpr-669058
ABSTRACT
Congenital glucose-galactose malabsorption(CGGM),also known as congenital glucose-ga-lactose intolerance syndrome,is a rare autosomal recessive hereditary disease.Domestic research about CGGM is rare and there was no discovery of the cases for this disease.This review summarizes the mechanism,clinical characteristics,diagnosis and treatment of CGGM.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Idioma:
Chinês
Revista:
International Journal of Pediatrics
Ano de publicação:
2017
Tipo de documento:
Artigo
Similares
MEDLINE
...
LILACS
LIS