 Glucosephosphate Dehydrogenase Deficiency
"Glucosephosphate Dehydrogenase Deficiency" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A disease-producing enzyme deficiency subject to many variants, some of which cause a deficiency of GLUCOSE-6-PHOSPHATE DEHYDROGENASE activity in erythrocytes, leading to hemolytic anemia.
| Descriptor ID |
D005955
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| MeSH Number(s) |
C15.378.071.141.150.480 C16.320.070.480 C16.320.565.202.402 C18.452.648.202.402
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| Concept/Terms |
Glucosephosphate Dehydrogenase Deficiency- Glucosephosphate Dehydrogenase Deficiency
- Deficiencies, Glucosephosphate Dehydrogenase
- Dehydrogenase Deficiencies, Glucosephosphate
- Dehydrogenase Deficiency, Glucosephosphate
- Deficiency, GPD
- Deficiencies, GPD
- GPD Deficiencies
- G6PD Deficiency
- Deficiencies, G6PD
- Deficiency, G6PD
- G6PD Deficiencies
- Glucose 6 Phosphate Dehydrogenase Deficiency
- Glucosephosphate Dehydrogenase Deficiencies
- GPD Deficiency
- Hemolytic Anemia Due to G6PD Deficiency
- Deficiency of Glucose-6-Phosphate Dehydrogenase
- Deficiency of Glucose 6 Phosphate Dehydrogenase
- Deficiency, Glucosephosphate Dehydrogenase
- Glucose-6-Phosphate Dehydrogenase Deficiency
- Deficiencies, Glucose-6-Phosphate Dehydrogenase
- Deficiency, Glucose-6-Phosphate Dehydrogenase
- Dehydrogenase Deficiencies, Glucose-6-Phosphate
- Dehydrogenase Deficiency, Glucose-6-Phosphate
- Glucose-6-Phosphate Dehydrogenase Deficiencies
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Below are MeSH descriptors whose meaning is more general than "Glucosephosphate Dehydrogenase Deficiency".
- Diseases [C]
- Hemic and Lymphatic Diseases [C15]
- Hematologic Diseases [C15.378]
- Anemia [C15.378.071]
- Anemia, Hemolytic [C15.378.071.141]
- Anemia, Hemolytic, Congenital [C15.378.071.141.150]
- Glucosephosphate Dehydrogenase Deficiency [C15.378.071.141.150.480]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Anemia, Hemolytic, Congenital [C16.320.070]
- Glucosephosphate Dehydrogenase Deficiency [C16.320.070.480]
- Metabolism, Inborn Errors [C16.320.565]
- Carbohydrate Metabolism, Inborn Errors [C16.320.565.202]
- Glucosephosphate Dehydrogenase Deficiency [C16.320.565.202.402]
- Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
- Metabolism, Inborn Errors [C18.452.648]
- Carbohydrate Metabolism, Inborn Errors [C18.452.648.202]
- Glucosephosphate Dehydrogenase Deficiency [C18.452.648.202.402]
Below are MeSH descriptors whose meaning is more specific than "Glucosephosphate Dehydrogenase Deficiency".
- Glucosephosphate Dehydrogenase Deficiency
- Favism
This graph shows the total number of publications written about "Glucosephosphate Dehydrogenase Deficiency" by people in this website by year, and whether "Glucosephosphate Dehydrogenase Deficiency" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2004 | 1 | 0 | 1 | | 2016 | 1 | 0 | 1 | | 2018 | 1 | 0 | 1 | | 2020 | 2 | 0 | 2 | | 2021 | 2 | 0 | 2 | | 2023 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Glucosephosphate Dehydrogenase Deficiency" by people in Profiles.
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Dziewulska KH, Reisz JA, Hay AM, D'Alessandro A, Zimring JC. Hemolysis and Metabolic Lesion of G6PD Deficient RBCs in Response to Dapsone Hydroxylamine in a Humanized Mouse Model. J Pharmacol Exp Ther. 2023 09; 386(3):323-330.
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Flaherty S, Strauch P, Maktabi M, Pybus BS, Reichard G, Walker LA, Rochford R. Mechanisms of 8-aminoquinoline induced haemolytic toxicity in a G6PDd humanized mouse model. J Cell Mol Med. 2022 07; 26(13):3675-3686.
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Roubinian NH, Reese SE, Qiao H, Plimier C, Fang F, Page GP, Cable RG, Custer B, Gladwin MT, Goel R, Harris B, Hendrickson JE, Kanias T, Kleinman S, Mast AE, Sloan SR, Spencer BR, Spitalnik SL, Busch MP, Hod EA. Donor genetic and nongenetic factors affecting red blood cell transfusion effectiveness. JCI Insight. 2022 01 11; 7(1).
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Sanna GD, Canonico ME, Siciliano R, Guarino S, Montereggi F, Ponti E, Corda G, Talanas G, Parodi G. Impact of glucose-6-phosphate dehydrogenase deficiency on the severity of coronary atherosclerosis in patients with acute coronary syndromes. J Cardiovasc Med (Hagerstown). 2021 Nov 01; 22(11):813-817.
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D'Alessandro A, Howie HL, Hay AM, Dziewulska KH, Brown BC, Wither MJ, Karafin M, Stone EF, Spitalnik SL, Hod EA, Francis RO, Fu X, Thomas T, Zimring JC. Hematologic and systemic metabolic alterations due to Mediterranean class II G6PD deficiency in mice. JCI Insight. 2021 07 22; 6(14).
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Tzounakas VL, Dzieciatkowska M, Anastasiadi AT, Karadimas DG, Vergaki A, Siourounis P, Stamoulis K, Papassideri IS, Kriebardis AG, D'Alessandro A, Antonelou MH. Red cell proteasome modulation by storage, redox metabolism and transfusion. Blood Transfus. 2022 01; 20(1):27-39.
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Francis RO, D'Alessandro A, Eisenberger A, Soffing M, Yeh R, Coronel E, Sheikh A, Rapido F, La Carpia F, Reisz JA, Gehrke S, Nemkov T, Thomas T, Schwartz J, Divgi C, Kessler D, Shaz BH, Ginzburg Y, Zimring JC, Spitalnik SL, Hod EA. Donor glucose-6-phosphate dehydrogenase deficiency decreases blood quality for transfusion. J Clin Invest. 2020 05 01; 130(5):2270-2285.
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Lauden SM, Chongwain S, Achidi A, Helm E, Cusick SE, Krug A, Slusher TM, Lund TC. Prevalence of glucose-6-phosphate dehydrogenase deficiency in Cameroonian blood donors. BMC Res Notes. 2019 Apr 02; 12(1):195.
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Karafin MS, Fu X, D'Alessandro A, Thomas T, Hod EA, Zimring JC, Field JJ, Francis RO. The clinical impact of glucose-6-phosphate dehydrogenase deficiency in patients with sickle cell disease. Curr Opin Hematol. 2018 11; 25(6):494-499.
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Wickham KS, Baresel PC, Marcsisin SR, Sousa J, Vuong CT, Reichard GA, Campo B, Tekwani BL, Walker LA, Rochford R. Single-Dose Primaquine in a Preclinical Model of Glucose-6-Phosphate Dehydrogenase Deficiency: Implications for Use in Malaria Transmission-Blocking Programs. Antimicrob Agents Chemother. 2016 10; 60(10):5906-13.
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