Creatine kinase and lactate dehydrogenase in type 2 glycogenesis (Pompe disease)

B. Gerson, John Michael Hemphill, R. C. Rock

Research output: Contribution to journalArticle

Abstract

At least 3 varieties of type 2 glycogenosis (Pompe disease) have been described, the most severe of which is an infantile form. The relationship between clinical manifestations, glycogen accumulation, and tissue damage has not been established. Serum levels of creatine kinase (CK; adenosine triphosphate:creatine phosphotransferase) lactate dehydrogenase (LDH; L-lactate:NAD oxidoreductase) and their isoenzyme fractions were used to identify and monitor myocardial damage in this study of an infant with type 2 glycogenosis diagnosed by light microscopy and tissue enzyme assay.

Original languageEnglish (US)
Pages (from-to)213-215
Number of pages3
JournalArchives of Pathology and Laboratory Medicine
Volume101
Issue number4
StatePublished - Dec 1 1977
Externally publishedYes

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Glycogen Storage Disease Type II
Creatine Kinase
L-Lactate Dehydrogenase
Creatine
Enzyme Assays
Glycogen
NAD
Isoenzymes
Microscopy
Oxidoreductases
Phosphotransferases
Adenosine Triphosphate
Light
Serum
lactate dehydrogenase 2

ASJC Scopus subject areas

  • Pathology and Forensic Medicine
  • Medical Laboratory Technology

Cite this

Creatine kinase and lactate dehydrogenase in type 2 glycogenesis (Pompe disease). / Gerson, B.; Hemphill, John Michael; Rock, R. C.

In: Archives of Pathology and Laboratory Medicine, Vol. 101, No. 4, 01.12.1977, p. 213-215.

Research output: Contribution to journalArticle

Gerson, B. ; Hemphill, John Michael ; Rock, R. C. / Creatine kinase and lactate dehydrogenase in type 2 glycogenesis (Pompe disease). In: Archives of Pathology and Laboratory Medicine. 1977 ; Vol. 101, No. 4. pp. 213-215.
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