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10.5152/tpa.2014.1071 http://scihub22266oqcxt.onion/10.5152/tpa.2014.1071 C4462281!4462281!26078655     free     free     free Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Turk+Pediatri+Ars 2014 ; 49 (2): 163-6 Nephropedia Template TP {{tp|p=26078655|t=2014. A rare cause of thrombocyte dysfunction: Hermansky-Pudlak syndrome |pdf=|usr=}}{{26078655}} gab.com Text A rare cause of thrombocyte dysfunction: Hermansky-Pudlak syndrome JO: Turk Pediatri Ars http://www.kidney.de/pget.php?&tw=1&pmid=26078655 #FOAvip 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, postoperative hemorrhage and gingival bleeding may be observed. Here we present 3 patients who were diagnosed with HPS in our clinic. In conclusion, HPS should be considered in all patients with ocular findings and albinism even though bleeding disorder is not described. Bleeding findings may be mild or unrecognized. Absence of secondary wave in platalet aggregation tests supports the diagnosis. Twit Text FOAVip A rare cause of thrombocyte dysfunction: Hermansky-Pudlak syndrome ????Turk Pediatri Ars http://www.kidney.de/pget.php?&tw=1&pmid=26078655 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26078655 #FOAvip English Wikipedia <ref>{{Cite pmid|26078655}}</ref> A rare cause of thrombocyte dysfunction: Hermansky-Pudlak syndrome #MMPMID26078655 Özdemir N; Çelik E; Ba?lar Z; Celkan T Turk Pediatri Ars 2014[Jun]; 49 (2): 163-6 PMID26078655show ga 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, postoperative hemorrhage and gingival bleeding may be observed. Here we present 3 patients who were diagnosed with HPS in our clinic. In conclusion, HPS should be considered in all patients with ocular findings and albinism even though bleeding disorder is not described. Bleeding findings may be mild or unrecognized. Absence of secondary wave in platalet aggregation tests supports the diagnosis. äA rare cause of thrombocyte dysfunction: Hermansky-Pudlak syndrome (epmc).pdf DeepDyve Pubget Overpricing