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searching for Mitochondrial DNA depletion syndrome 7 found (25 total)

alternate case: mitochondrial DNA depletion syndrome

AGK (gene) (1,379 words) [view diff] exact match in snippet view article

lysophosphatidic acids. Defects in this gene have been associated with mitochondrial DNA depletion syndrome 10. Diseases associated with AGK include cataracts and cardiomyopathy

Mitochondrial neurogastrointestinal encephalopathy syndrome (800 words) [view diff] case mismatch in snippet view article find links to article

ISSN 0006-8950. PMC 3212717. PMID 21933806. "OMIM Entry - # 603041 - MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1". omim.org. Retrieved 2015-12-02.

List of causes of hypoglycemia (1,265 words) [view diff] exact match in snippet view article find links to article

deficiency Mesothelioma Methylmalonic acidemia Mitiglinide Mitochondrial DNA depletion syndrome, hepatocerebral form Mitochondrial trifunctional protein

Kinase (3,805 words) [view diff] exact match in snippet view article find links to article

in the thymidine kinase gene may have a certain type of mitochondrial DNA depletion syndrome, a disease that leads to death in early childhood. Wikimedia

List of OMIM disorder codes (18,877 words) [view diff] exact match in snippet view article find links to article

FASTKD2 Mitochondrial DNA depletion syndrome, encephalomyopathic form, with methylmalonic aciduria; 612073; SUCLA2 Mitochondrial DNA depletion syndrome, encephalomyopathic

Extrachromosomal DNA (5,349 words) [view diff] exact match in snippet view article find links to article

ES, Wong LJ (July 2010). "Quantitative evaluation of the mitochondrial DNA depletion syndrome". Clinical Chemistry. 56 (7): 1119–27. doi:10.1373/clinchem

Thymidine kinase (11,106 words) [view diff] exact match in snippet view article find links to article

Mutations in the gene for TK2 lead to a myopathic form of mitochondrial DNA depletion syndrome. Another reason for TK 2 deficiency may be oxidative stress