HEREDITARY FRUCTOSE INTOLERANCE IN A PATIENT WITH PHENYLKETONURIA

被引：0

作者：

COSKUN, T

OZALP, I

TEKINALP, G

机构：

来源：

TURKISH JOURNAL OF PEDIATRICS | 1991年 / 33卷 / 03期

关键词：

PHENYLKETONURIA; HEREDITARY FRUCTOSE INTOLERANCE;

D O I：

暂无

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

Classical phenylketonuria (PKU) and hereditary fructose intolerance (HFI) are two inborn errors of metabolism that have an autosomal recessive mode of inheritance. In this paper, we described a 3 - year - old girl with PKU and HFI. The occurrence of these two defects in the same patient is thought to be fortuitous and not genetically related since this is the first reported case and the statistical probability of such an occurrence is very low.

引用

页码：181 / 184

页数：4