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
|
| MeSH Number(s) |
C15.378.071.141.150.480 C16.320.070.480 C16.320.565.202.402 C18.452.648.202.402
|
| 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
|
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.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2007 | 1 | 0 | 1 |
| 2013 | 1 | 0 | 1 |
| 2019 | 1 | 0 | 1 |
| 2020 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
| 2024 | 1 | 0 | 1 |
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Below are the most recent publications written about "Glucosephosphate Dehydrogenase Deficiency" by people in Profiles.
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Iyer NS, Mossayebi MH, Gao TJ, Haizler-Cohen L, Di Mascio D, McLaren RA, Al-Kouatly HB. Glucose-6-phosphate dehydrogenase deficiency as a cause for nonimmune hydrops fetalis and severe fetal anemia: A systematic review. Mol Genet Genomic Med. 2024 Jul; 12(7):e2491.
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Pankey AN, Chandar A, Isaacson G. Safety of Ibuprofen in Children With G6PD Deficiency: A Systematic Review. Laryngoscope. 2022 06; 132(6):1300-1305.
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Benavides N, Spessott WA, Sanmillan ML, Vargas M, Livingston MS, Erickson N, Pozos TC, McCormick ME, Scharrig E, Messinger YH, Giraudo CG. STXBP2-R190C Variant in a Patient With Neonatal Hemophagocytic Lymphohistiocytosis (HLH) and G6PD Deficiency Reveals a Critical Role of STXBP2 Domain 2 on Granule Exocytosis. Front Immunol. 2020; 11:545414.
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Harcke SJ, Rizzolo D, Harcke HT. G6PD deficiency: An update. JAAPA. 2019 Nov; 32(11):21-26.
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Raj V, Chism K, Minckler MR, Denysenko L. Catatonia and glucose-6-phosphate dehydrogenase deficiency: a report of two cases and a review. Psychosomatics. 2014 Jan-Feb; 55(1):92-7.
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Schutzman DL, Porat R. Glucose-6-phosphate dehydrogenase deficiency: another risk factor for necrotizing enterocolitis? J Pediatr. 2007 Oct; 151(4):435-7.
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Vanella A, Campisi A, Castorina C, Sorrenti V, Attaguile G, Samperi P, Azzia N, Di Giacomo C, Schilir? G. Antioxidant enzymatic systems and oxidative stress in erythrocytes with G6PD deficiency: effect of deferoxamine. Pharmacol Res. 1991 Jul; 24(1):25-31.
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Vanella A, Gorgone G, Cavallaro N, Castorina C, Campisi A, Di Giacomo C, Bousquet E, Li Volti S, Mollica F. Superoxide dismutase activity and reduced glutathione content in cataractous lens of patients with glucose-6-phosphate dehydrogenase deficiency. Ophthalmic Paediatr Genet. 1987 Nov; 8(3):191-5.
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Pacheco J, Gabuzda TG, Jackson L. Letter: Erythroleukemia with Philadelphia chromosome. JAMA. 1973 Nov 12; 226(7):787.
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Siniscalco M, Klinger HP, Eagle H, Koprowski H, Fujimoto WY, Seegmiller JE. Evidence for intergenic complementation in hybrid cells derived from two human diploid strains each carrying an X-linked mutation. Proc Natl Acad Sci U S A. 1969 Mar; 62(3):793-9.