[Heterozygous NADH-methemoglobin reductase defect with methemoglobinemia in an infant (author's transl)]. 1973

I Witt, and J Gunkel, and G Seibert, and H Wehinger, and L Schuchmann, and W Künzer

UI MeSH Term Description Entries
D007231 Infant, Newborn An infant during the first 28 days after birth. Neonate,Newborns,Infants, Newborn,Neonates,Newborn,Newborn Infant,Newborn Infants
D008661 Metabolism, Inborn Errors Errors in metabolic processes resulting from inborn genetic mutations that are inherited or acquired in utero. Inborn Errors of Metabolism,Metabolism Errors, Inborn,Error, Inborn Metabolism,Errors Metabolism, Inborn,Errors Metabolisms, Inborn,Errors, Inborn Metabolism,Inborn Errors Metabolism,Inborn Errors Metabolisms,Inborn Metabolism Error,Inborn Metabolism Errors,Metabolism Error, Inborn,Metabolism Inborn Error,Metabolism Inborn Errors,Metabolisms, Inborn Errors
D008706 Methemoglobin Ferrihemoglobin
D008708 Methemoglobinemia The presence of methemoglobin in the blood, resulting in cyanosis. A small amount of methemoglobin is present in the blood normally, but injury or toxic agents convert a larger proportion of hemoglobin into methemoglobin, which does not function reversibly as an oxygen carrier. Methemoglobinemia may be due to a defect in the enzyme NADH methemoglobin reductase (an autosomal recessive trait) or to an abnormality in hemoglobin M (an autosomal dominant trait). (Dorland, 27th ed) Methemoglobinemias
D009247 NADH, NADPH Oxidoreductases A group of oxidoreductases that act on NADH or NADPH. In general, enzymes using NADH or NADPH to reduce a substrate are classified according to the reverse reaction, in which NAD+ or NADP+ is formally regarded as an acceptor. This subclass includes only those enzymes in which some other redox carrier is the acceptor. (Enzyme Nomenclature, 1992, p100) EC 1.6. Oxidoreductases, NADH, NADPH,NADPH Oxidoreductases NADH,Oxidoreductases NADH, NADPH
D010375 Pedigree The record of descent or ancestry, particularly of a particular condition or trait, indicating individual family members, their relationships, and their status with respect to the trait or condition. Family Tree,Genealogical Tree,Genealogic Tree,Genetic Identity,Identity, Genetic,Family Trees,Genealogic Trees,Genealogical Trees,Genetic Identities,Identities, Genetic,Tree, Family,Tree, Genealogic,Tree, Genealogical,Trees, Family,Trees, Genealogic,Trees, Genealogical
D003968 Diarrhea, Infantile DIARRHEA occurring in infants from newborn to 24-months old. Infantile Diarrhea,Diarrheas, Infantile,Infantile Diarrheas
D004912 Erythrocytes Red blood cells. Mature erythrocytes are non-nucleated, biconcave disks containing HEMOGLOBIN whose function is to transport OXYGEN. Blood Cells, Red,Blood Corpuscles, Red,Red Blood Cells,Red Blood Corpuscles,Blood Cell, Red,Blood Corpuscle, Red,Erythrocyte,Red Blood Cell,Red Blood Corpuscle
D005260 Female Females
D005319 Fetal Hemoglobin The major component of hemoglobin in the fetus. This HEMOGLOBIN has two alpha and two gamma polypeptide subunits in comparison to normal adult hemoglobin, which has two alpha and two beta polypeptide subunits. Fetal hemoglobin concentrations can be elevated (usually above 0.5%) in children and adults affected by LEUKEMIA and several types of ANEMIA. Hemoglobin F,Hemoglobin, Fetal

Related Publications

I Witt, and J Gunkel, and G Seibert, and H Wehinger, and L Schuchmann, and W Künzer
September 1976, La Pediatria,
I Witt, and J Gunkel, and G Seibert, and H Wehinger, and L Schuchmann, and W Künzer
December 1984, International journal of leprosy and other mycobacterial diseases : official organ of the International Leprosy Association,
I Witt, and J Gunkel, and G Seibert, and H Wehinger, and L Schuchmann, and W Künzer
December 1988, Pediatria polska,
I Witt, and J Gunkel, and G Seibert, and H Wehinger, and L Schuchmann, and W Künzer
June 1980, Masui. The Japanese journal of anesthesiology,
I Witt, and J Gunkel, and G Seibert, and H Wehinger, and L Schuchmann, and W Künzer
November 1974, The Indian journal of medical research,
I Witt, and J Gunkel, and G Seibert, and H Wehinger, and L Schuchmann, and W Künzer
June 1972, The Journal of clinical investigation,
I Witt, and J Gunkel, and G Seibert, and H Wehinger, and L Schuchmann, and W Künzer
January 1972, Marseille medical,
I Witt, and J Gunkel, and G Seibert, and H Wehinger, and L Schuchmann, and W Künzer
January 1971, The Journal of clinical investigation,
I Witt, and J Gunkel, and G Seibert, and H Wehinger, and L Schuchmann, and W Künzer
January 1984, Biomedica biochimica acta,
I Witt, and J Gunkel, and G Seibert, and H Wehinger, and L Schuchmann, and W Künzer
July 1974, Blut,
Copied contents to your clipboard!