Bernard Soulier Syndrome is an autosomal recessive inherited platelet function disorder characterized by mild thrombocytopenia abnormally large platelets on peripheral blood smear It is clinically manifested by epistaxis and purpura ranging from mild to moderate degree In this article an 8 year old case with Bernard Soulier syndrome diagnosed after epistaxis and purpura for two days has been presented Key words: Bernard Soulier Syndrome Thrombocytopenia
Bernard Soulier Sendromu hafif dereceli trombositopeni periferde dev trombositlerle karakterli otozomal resesif kalıtılan trombosit fonksiyon bozukluğudur Klinik olarak epistaksis ve orta ile ağır dereceler arasında değişen purpurik kanamalarla seyreder Bu yazıda iki gündür spontan burun kanaması ve yaygın peteşial döküntüleri olan 8 yaşında Bernard Soulier Sendrom lu erkek bir hasta takdim edilmiştir Anahtar kelimeler: Bernard Soulier Sendromu Trombositopeni
Primary Language | Turkish |
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Journal Section | When the Turkish word exists |
Authors | |
Publication Date | September 1, 1997 |
Published in Issue | Year 1997 Volume: 32 Issue: 3 |