Rhabdomyolysis in early-onset very long-chain acyl-CoA dehydrogenase deficiency despite normal glucose after fasting

被引：15

作者：

Engbers, HM

Dorland, L

De Sain, MGM

Eskes, PF

Visser, G

机构：

[1] Wilhelmina Childrens Hosp, Dept Metab Dis, NL-3508 AB Utrecht, Netherlands

[2] Meander Hosp, Amersfoort, Netherlands

来源：

JOURNAL OF INHERITED METABOLIC DISEASE | 2005年 / 28卷 / 06期

关键词：

D O I：

10.1007/s10545-005-0190-y

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

A patient with very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency presented in the neonatal period with hypoketotic hypoglycaemia and at the age of 1 year with rhabdomyolysis and normal glucose after fasting. Rhabdomyolysis may occur in the absence of hypoglycaemia in young infants as well as in older patients.

引用

页码：1151 / 1152

页数：2