PedAM
Pediatric Disease Annotations & Medicines
| Disease | thrombasthenia |
| Phenotype | C0042974|von willebrand disease |
| Sentences | 2 |
| PubMedID- 20147343 | Coinheritance of severe von willebrand disease with glanzmann thrombasthenia. |
| PubMedID- 24418945 | We report a case of glanzmann thrombasthenia combined with type 2n von willebrand disease (vwd), a variant characterized by an impaired capacity of fviii to bind von willebrand factor (vwf), which results in an autosomally transmitted reduction in circulating fviii levels. |
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