| A case of congenital lactic acidosis. |
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Suk Min Choi1, Myeong Ku Cho1, Dong Hwan Lee1, Sang Jhoo Lee1, Kikumaro Aoki2, Shuichi Yamaguchi3 |
1Department of Pediatrics, College of Medicine, Soon Chum Hyang University, Seoul, Korea
2Aiiku Maternal & Child Health Center, Tokyo, Japan
3Saitama Children fs Medical Center, Saitama, Japan |
| Congenital Lactic Acidosis 1 례 |
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최석민1, 조명구1, 이동환1, 이상주1, 靑木菊磨2, 山□修一3 |
1순천향대학교 의과대학 소아과학교실
2日本 母子愛育合 銳合母子保健 센타
3日本 倚玉県立 小児医療 센타 |
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Received: 13 August 1990 • Accepted: 17 October 1990 |
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| Abstract |
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The congenital lactic acidosis represent a sizable group of metabolic disorders.
They are in all likelihood genetically determined, and they are clearly heterogenous. They may be
considered broadly as disorders of pyruvate metabolism in which there are two general categories:
defects in gluconeogenesis and defects in pyruvate oxidation.
We experienced a case of congenital lactic acidosis in neonate who was diagnosed by urinary
organic acid analysis.
A brief review of related literature is also presented. |
| Key Words:
Congenital lactic acidosis |
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