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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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Bibliografiska uppgifter
I publikationen:Turk Pediatri Ars
Huvudupphovsmän: Özdemir, Nihal, Çelik, Emre, Başlar, Zafer, Celkan, Tiraje
Materialtyp: Artigo
Språk:Inglês
Publicerad: Turkish Pediatrics Association 2014
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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