"Thrombasthenia" 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 congenital bleeding disorder with prolonged bleeding time, absence of aggregation of platelets in response to most agents, especially ADP, and impaired or absent clot retraction. Platelet membranes are deficient in or have a defect in the glycoprotein IIb-IIIa complex (PLATELET GLYCOPROTEIN GPIIB-IIIA COMPLEX).
| Descriptor ID |
D013915
|
| MeSH Number(s) |
C15.378.100.100.820 C15.378.140.810 C15.378.463.810 C16.320.099.820
|
| Concept/Terms |
Thrombasthenia- Thrombasthenia
- Thrombasthenias
- Thrombasthenia of Glanzmann and Naegeli
- Glanzmann Thrombasthenia
- Thrombasthenia, Glanzmann
Glanzmann Thrombasthenia, Type A- Glanzmann Thrombasthenia, Type A
- Platelet Fibrinogen Receptor, Deficiency of
- Platelet Glycoprotein IIb-IIIa Deficiency
- Platelet Glycoprotein IIb IIIa Deficiency
- Glycoprotein Complex IIb-IIIa, Deficiency Of
- Glycoprotein Complex IIb IIIa, Deficiency Of
- GP IIb-IIIa Complex, Deficiency Of
- GP IIb IIIa Complex, Deficiency Of
- Deficiency of GP 2b 3a Complex
- Platelet Glycoprotein 2b-3a Deficiency
- Platelet Glycoprotein 2b 3a Deficiency
|
Below are MeSH descriptors whose meaning is more general than "Thrombasthenia".
Below are MeSH descriptors whose meaning is more specific than "Thrombasthenia".
This graph shows the total number of publications written about "Thrombasthenia" by people in this website by year, and whether "Thrombasthenia" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2017 | 1 | 1 | 2 |
| 2018 | 3 | 0 | 3 |
| 2020 | 1 | 0 | 1 |
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Below are the most recent publications written about "Thrombasthenia" by people in Profiles.
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COVID-19 in a pediatric patient with Glanzmann thrombasthenia. Pediatr Blood Cancer. 2020 10; 67(10):e28662.
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Missed at first Glanz: Glanzmann thrombasthenia initially misdiagnosed as Von Willebrand Disease. Transfus Apher Sci. 2019 Feb; 58(1):58-60.
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How we treat the platelet glycoprotein defects; Glanzmann thrombasthenia and Bernard Soulier syndrome in children and adults. Br J Haematol. 2018 09; 182(5):621-632.
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Perioperative management of a patient with Glanzmann thrombasthenia undergoing a coronary artery bypass graft surgery: a case report. Blood Coagul Fibrinolysis. 2018 Apr; 29(3):327-329.
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Molecular characterization of Glanzmann's thrombasthenia in Iran: identification of three novel mutations. Blood Coagul Fibrinolysis. 2017 Dec; 28(8):681-686.
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Diagnosis of inherited platelet disorders on a blood smear: a tool to facilitate worldwide diagnosis of platelet disorders. J Thromb Haemost. 2017 07; 15(7):1511-1521.
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[Hemorrhage of upper digestive and respiratory tracts in children. A clinical, biological and therapeutic approach]. Ann Otolaryngol Chir Cervicofac. 1993; 110(7):405-14.