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Results 1 - 4 of 4 for Fatal multiple mitochondrial dysfunctions syndrome
  1. BOLA3 gene 
    ... dehydrogenase, or alpha-ketoglutarate dehydrogenase leads to potentially fatal lactic acidosis, encephalopathy, and other signs and symptoms of multiple mitochondrial dysfunctions syndrome. In some affected individuals, impairment of the glycine ...
    https://medlineplus.gov/genetics/gene/bola3 - Genetics
  2. NFU1 gene 
    ... dehydrogenase, or alpha-ketoglutarate dehydrogenase leads to potentially fatal lactic acidosis, encephalopathy, and other signs and symptoms of multiple mitochondrial dysfunctions syndrome. In some affected individuals, impairment of the glycine ...
    https://medlineplus.gov/genetics/gene/nfu1 - Genetics
  3. FBXL4 gene 
    ... found to cause FBXL4-related encephalomyopathic mtDNA depletion syndrome. This condition affects multiple body systems and is often fatal in early childhood. It is primarily associated with brain dysfunction combined with muscle weakness (encephalomyopathy).Many of the ...
    https://medlineplus.gov/genetics/gene/fbxl4 - Genetics
  4. FH gene 
    ... Gottlieb E. Succinate dehydrogenase and fumarate hydratase: linking mitochondrial dysfunction and cancer. Oncogene. 2006 Aug 7;25(34): ...
    https://medlineplus.gov/genetics/gene/fh - Genetics