Familial chronic acidosis due to an error in lactate and pyruvate metabolism.

Canadian Medical Association journal ·Vol. 97 ·No. 13 ·1967-09-23 ·Pages 773-9

Haworth JC, Ford JD, Younoszai MK

Abstract

暂无摘要

MeSH Terms

Acidosis/complications,genetics Female Humans Indians, North American Infant Intellectual Disability/complications Ketoglutaric Acids/urine Lactates/blood Male Metabolism, Inborn Errors Muscles/metabolism Muscular Diseases/complications Neurologic Manifestations Obesity/complications Ontario Pyruvates/blood Seizures/complications

Chemicals

Ketoglutaric Acids Lactates Pyruvates

Authors & Affiliations

3 authors, click to expand affiliations / ORCID

Haworth J C

Ford J D

Younoszai M K

References (5)

5 references, click to expand

Lactate metabolism. Studies of a child with a serious congenital deviation.
J Pediatr. 1962 Aug;61:165-80 PMID: 13905026
FAMILIAL INFANTILE LACTIC ACIDOSIS.
J Pediatr. 1965 Jun;66:1004-16 PMID: 14288452
Isozymes: biological and clinical significance.
Pediatrics. 1966 Jan;37(1):120-31 PMID: 5323002
Lactic acidosis with necrotizing encephalopathy in two sibs.
Arch Dis Child. 1965 Oct;40(213):492-501 PMID: 5829993
THE METABOLISM OF ALPHA-KETO ACIDS IN VON GIERKE'S DISEASE.
Clin Chim Acta. 1964 Jun;9:587-9 PMID: 14187080

Article Info

Journal

Canadian Medical Association journal

Abbr.

Can Med Assoc J

ISSN

0008-4409

Published

1967-09-23

Pages

773-9

Language

English

Region

Canada

NLM ID

0414110

PMCID

PMC1923319

Subset

External Links

PubMed source PMC Full Text

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Familial chronic acidosis due to an error in lactate and pyruvate metabolism.

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