Thiamine-Responsive Congenital Lactic Acidosis Without MC

J Gordon Millichap

doi:10.15844/pedneurbriefs-19-8-3

Thiamine-Responsive Congenital Lactic Acidosis Without MC

Pediatric Neurology Briefs

Volume 19 (2005): Issue 8

By: J Gordon Millichap

Open Access

|Aug 2005

Abstract

Six infants with thiamine-responsive congenital lactic acidosis (CLA), normal pyruvate dehydrogenase complex activity, and no evidence of mitochondrial encephalomyopathy, are reported from Tottori University, Yonago; National Children’s Medical Center, Tokyo, and other centers in Japan.

References

Toyoshima M Oka A Egi Y Yamamoto T Onozuka M Nosaka K Thiamine-responsive congenital lactic acidosis: clinical and biochemical studies Pediatr Neurol 2005 Aug 33 2 98 104 10.1016/j.pediatrneurol.2005.02.007 16087053
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-19-8-3 | Journal eISSN: 2166-6482

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Language: English

Page range: 58 - 59

Published on: Aug 1, 2005

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Congenital Lactic Acidosis,

Mitochondrial Encephalomyopathy,

Cardiomyopathy

© 2005 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 19 (2005): Issue 8