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PedAM

Pediatric Disease Annotations & Medicines




Disease von willebrand disease
Phenotype C0040015|glanzmann thrombasthenia
Sentences 2
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.
PubMedID- 20147343 Coinheritance of severe von willebrand disease with glanzmann thrombasthenia.

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