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A rare cause of thrombocyte dysfunction: Hermansky-Pudlak syndrome
Hermansky-Pudlak syndrome (HPS) is an autosomal recessive disease characterized with oculocutaneous albinism and platelet aggregation disorder. The clinical picture is highly variable and patients may present with different complaints., Ecchymoses usually develop in childhood; epistaxis, postoperati...
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| I publikationen: | Turk Pediatri Ars |
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| Huvudupphovsmän: | , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Turkish Pediatrics Association
2014
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4462281/ https://ncbi.nlm.nih.gov/pubmed/26078655 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5152/tpa.2014.1071 |
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