"Bernard-Soulier Syndrome" 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 familial coagulation disorder characterized by a prolonged bleeding time, unusually large platelets, and impaired prothrombin consumption.
| Descriptor ID |
D001606
|
| MeSH Number(s) |
C15.378.100.100.080 C15.378.140.120 C15.378.463.080 C16.320.099.080
|
| Concept/Terms |
Bernard-Soulier Syndrome- Bernard-Soulier Syndrome
- Bernard Soulier Syndrome
- Syndrome, Bernard-Soulier
- Giant Platelet Syndrome
- Platelet Syndromes, Giant
- Syndrome, Giant Platelet
- Syndromes, Giant Platelet
Deficiency of Platelet Glycoprotein 1b- Deficiency of Platelet Glycoprotein 1b
- Von Willebrand Factor Receptor Deficiency
- Platelet Glycoprotein Ib Deficiency
- Platelet Glycoprotein 1b, Deficiency of
- Glycoprotein Ib, Platelet, Deficiency Of
|
Below are MeSH descriptors whose meaning is more general than "Bernard-Soulier Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Bernard-Soulier Syndrome".
This graph shows the total number of publications written about "Bernard-Soulier Syndrome" by people in this website by year, and whether "Bernard-Soulier Syndrome" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2000 | 1 | 0 | 1 |
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Below are the most recent publications written about "Bernard-Soulier Syndrome" by people in Profiles.
-
Bernard-Soulier syndrome: common ancestry in two African American families with the GP Ib alpha Leu129Pro mutation. Am J Hematol. 2000 Oct; 65(2):141-8.