Molecular identification of a rare hemoglobin variant, Hb J-Iran [beta77(EF1)His->Asp], in Denizli province of TurkeyAylin Köseler1, Ayfer Atalay1, Hasan Koyuncu2, Berna Turgut2, Anzel Bahadır1, Erol Ömer Atalay11Department Of Biophysics, Pamukkale University Faculty Of Medicine, Denizli, Turkey
2Turkish Ministry Of Health, Hemoglobinopathy Center, Denizli, Turkey
Hb J-Iran [beta77(EF1)His-Asp], a rare hemoglobin variant that does not present health problems, was reported for the first time in the Turkish population in 1986. Our case is the fourth case reported in Turkey and the first case from the Denizli province. Keywords: Hb J-Iran, abnormal hemoglobin
--Aylin Köseler1, Ayfer Atalay1, Hasan Koyuncu2, Berna Turgut2, Anzel Bahadır1, Erol Ömer Atalay11Department Of Biophysics, Pamukkale University Faculty Of Medicine, Denizli
2Turkish Ministry Of Health, Hemoglobinopathy Center, Denizli
Hb J-Iran [beta77(EF1)His-Asp] herhangi bir sağlık sorunu yaratmayan nadir hemoglobin türlerinden olup Türkiye’de ilk kez 1986 yılında bildirilmiştir. Bu çalışmada sunulan heterozigot olgu ülkemizde bildirilen dördüncü, Denizli yöresinde ise ilk olgu olma özelliğini taşımaktadır. Anahtar Kelimeler: Hb J-Iran, anormal hemoglobin
Aylin Köseler, Ayfer Atalay, Hasan Koyuncu, Berna Turgut, Anzel Bahadır, Erol Ömer Atalay. Molecular identification of a rare hemoglobin variant, Hb J-Iran [beta77(EF1)His->Asp], in Denizli province of Turkey. Turk J Hematol. 2006; 23(3): 164-166
Corresponding Author: Aylin Köseler, Türkiye |
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