Mitochondrial Complex III Deficiency

Networked: 10 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results

Macromolecular Substances: 97
- Multiprotein Complexes: 125
  - Multienzyme Complexes: 8
    - Succinate Cytochrome c Oxidoreductase: 31
      - Electron Transport Complex III: 458
        Mitochondrial Complex III Deficiency: 10
Enzymes and Coenzymes: 1
- Enzymes: 152586
  - Oxidoreductases: 13671
    - Succinate Cytochrome c Oxidoreductase: 31
      - Electron Transport Complex III: 458
        Mitochondrial Complex III Deficiency: 10
  - Multienzyme Complexes: 8
    - Electron Transport Chain Complex Proteins
      - Succinate Cytochrome c Oxidoreductase: 31
        Electron Transport Complex III: 458
        Mitochondrial Complex III Deficiency: 10
Amino Acids, Peptides, and Proteins: 1
- Proteins: 484843
Nutritional and Metabolic Diseases: 15
- Metabolic Diseases: 10142
  - Mitochondrial Diseases: 21919
    - Mitochondrial Complex III Deficiency: 10

Experts

1.	Eminoğlu, Fatma Tuba: 1 article (02/2022)
2.	Ezgü, Fatih: 1 article (02/2022)
3.	Koç Yekedüz, Merve: 1 article (02/2022)
4.	Köse, Engin: 1 article (02/2022)
5.	Öncül, Ümmühan: 1 article (02/2022)
6.	Du, Chen: 1 article (01/2020)
7.	Feichtinger, René G: 1 article (01/2020)
8.	Gusic, Mirjana: 1 article (01/2020)
9.	Lee, Chae-Young: 1 article (01/2020)
10.	Lorenz, Norbert: 1 article (01/2020)

Related Diseases

1.	Stroke (Strokes) 01/01/2018 - "Novel Homozygous Variant in TTC19 Causing Mitochondrial Complex III Deficiency with Recurrent Stroke-Like Episodes: Expanding the Phenotype." 01/01/2023 - "LYRM7-associated mitochondrial complex III deficiency with non-cavitating leukoencephalopathy and stroke-like episodes."
2.	Hypoglycemia (Reactive Hypoglycemia) 02/01/2022 - "In this paper, we present a patient with mitochondrial complex III deficiency, nuclear type 3, UQCRB variant associated with acute hypoglycemia and lactic acidosis episodes. " 02/01/2022 - "To date, mitochondrial complex III deficiency, nuclear type 3 attributable to a pathogenic variant of the UQCRB gene (MIM 615158) has been identified in only 2 pediatric patients; both presented with hypoglycemia and lactic acidosis. " 07/01/2017 - "UQCRC2 mutation in a patient with mitochondrial complex III deficiency causing recurrent liver failure, lactic acidosis and hypoglycemia."
3.	Lactic Acidosis 02/01/2022 - "In this paper, we present a patient with mitochondrial complex III deficiency, nuclear type 3, UQCRB variant associated with acute hypoglycemia and lactic acidosis episodes. " 02/01/2022 - "To date, mitochondrial complex III deficiency, nuclear type 3 attributable to a pathogenic variant of the UQCRB gene (MIM 615158) has been identified in only 2 pediatric patients; both presented with hypoglycemia and lactic acidosis. " 07/01/2017 - "UQCRC2 mutation in a patient with mitochondrial complex III deficiency causing recurrent liver failure, lactic acidosis and hypoglycemia."
4.	Leukoencephalopathies 01/01/2023 - "LYRM7-associated mitochondrial complex III deficiency with non-cavitating leukoencephalopathy and stroke-like episodes."
5.	Liver Failure 07/01/2017 - "UQCRC2 mutation in a patient with mitochondrial complex III deficiency causing recurrent liver failure, lactic acidosis and hypoglycemia."

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