Heterozygosity for the Common LCHAD Mutation (1528G>C) Is Not a Major Cause of HELLP Syndrome and the Prevalence of the Mutation in the Dutch Population Is Low-Reference-Cited by-同舟云学术

Heterozygosity for the Common LCHAD Mutation (1528G>C) Is Not a Major Cause of HELLP Syndrome and the Prevalence of the Mutation in the Dutch Population Is Low

Published:2000-08 Issue:2 Volume:48 Page:151-154
ISSN:0031-3998
Container-title:Pediatric Research
language:
Short-container-title:Pediatr Res

Author:

Den Boer Margarethe E J,Ijlst Lodewijk,Wijburg Frits A,Oostheim Wendy,Van Werkhoven Michiel A,Van Pampus Marielle G,Heymans Hugo S A,Wanders Ronald J A

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Reference27 articles.

1. Long-chain 3-hydroxyacyl–coenzyme A dehydrogenase deficiency with the G1528C mutation: Clinical presentation of thirteen patients

2. The clinical spectrum of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency

3. Peripheral sensory-motor polyneuropathy, pigmentary retinopathy, and fatal cardiomyopathy in long-chain 3-hydroxy-acyl-CoA dehydrogenase deficiency

4. Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

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