摘要
先天性葡萄糖-半乳糖吸收不良(CGGM)又称先天性葡萄糖-半乳糖不耐受症,是一种罕见的常染色体隐性遗传性疾病,国内研究与发现者甚少,至今国内未见本病的病例报道.该文就先天性葡萄糖-半乳糖吸收不良的发生机制、临床特点、诊断及治疗作一综述.
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.
出处
《国际儿科学杂志》
2017年第10期663-666,共4页
International Journal of Pediatrics
