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Methemoglobin Reductase Deficiency
Also Known As:
NADPH-Dependent Methemoglobin Reductase Deficiency; TPNH-Methemoglobin Reductase Deficiency
Networked:
7
relevant articles (
0
outcomes,
0
trials/studies)
Disease Context: Research Results
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
Inborn Genetic Diseases: 11939
Inborn Errors Metabolism: 1162
Methemoglobin Reductase Deficiency: 7
Nutritional and Metabolic Diseases: 15
Metabolic Diseases: 10142
Inborn Errors Metabolism: 1162
Methemoglobin Reductase Deficiency: 7
Enzymes and Coenzymes: 1
Enzymes: 152586
Oxidoreductases: 13671
NADPH Oxidoreductases NADH
Cytochrome Reductases: 1
Cytochrome-B(5) Reductase: 114
Methemoglobin Reductase Deficiency: 7
Amino Acids, Peptides, and Proteins: 1
Proteins: 484843
Flavoproteins: 234
Cytochrome-B(5) Reductase: 114
Methemoglobin Reductase Deficiency: 7
Related Diseases
1.
Congenital Methemoglobinemia
2.
Methemoglobinemia
3.
Hemolysis
4.
Hemoglobinopathies
5.
Glucosephosphate Dehydrogenase Deficiency
Drugs and Biologics
Drugs and Important Biological Agents (IBA) related to Methemoglobin Reductase Deficiency:
1.
Methemoglobin
IBA
11/01/1994 - "
Subsequent analysis revealed 49.6% methemoglobin (normal, 0 to 1.1%), resulting from erythrocyte methemoglobin reductase deficiency (21% of normal activity).
"
05/01/1999 - "
Among the causes of life-long cyanosis are congenital methemoglobinemia due to M hemoglobins, congenital methemoglobinemia due to methemoglobin reductase deficiency, a small number of low oxygen affinity hemoglobins, and a small number of unstable hemoglobins that spontaneously form methemoglobin in vivo at an accelerated rate.
"
2.
Sodium Nitrite
IBA
10/01/1985 - "
Both cytochemical detection of G6PD-deficient cells in a female heterozygote for G6PD deficiency and the screening test for a methemoglobin reductase deficiency could be performed with butylnitrite as well as with sodium nitrite.
"
3.
Oxygen (Dioxygen)
IBA
05/01/1999 - "
Among the causes of life-long cyanosis are congenital methemoglobinemia due to M hemoglobins, congenital methemoglobinemia due to methemoglobin reductase deficiency, a small number of low oxygen affinity hemoglobins, and a small number of unstable hemoglobins that spontaneously form methemoglobin in vivo at an accelerated rate.
"
4.
NAD (NADH)
IBA
01/01/1972 - "
[Congenital methemoglobinemia due to NADH (DPNH) dependent methemoglobin reductase deficiency].
"
5.
Hemoglobins (Hemoglobin)
IBA
05/01/1999 - "
Among the causes of life-long cyanosis are congenital methemoglobinemia due to M hemoglobins, congenital methemoglobinemia due to methemoglobin reductase deficiency, a small number of low oxygen affinity hemoglobins, and a small number of unstable hemoglobins that spontaneously form methemoglobin in vivo at an accelerated rate.
"
6.
Enzymes
IBA
11/01/1967 - "
TPNH-methemoglobin reductase deficiency: a new red-cell enzyme defect.
"
7.
Dapsone
FDA Link
08/01/1981 - "
Dapsone-induced methemoglobinemia and hemolysis in the presence of familial hemoglobinopathy Hasharon and familial methemoglobin reductase deficiency.
"
8.
Ascorbic Acid (Vitamin C)
FDA Link
Generic
10/01/1977 - "
In methemoglobinemic conditions caused by toxic effects or by congenital methemoglobin reductase deficiency treatment with ascorbic acid is possible.
"