COMPOUND HETEROZYGOSITY FOR HB C/+ β-THALASSAEMIA. A CASE PRESENTATION

被引：0
|
作者：
Theodoridou, S. [1 ]
Alemayehu, M. [1 ]
Ganta, S. [1 ]
Tsalidou, M. [1 ]
Katsimpourlia, E. [1 ]
Perperidou, P. [1 ]
Karakasidou, O. [1 ]
Aletra, V. [1 ]
Papaioannou, G. [1 ]
机构：
[1] Hippokrateion Hosp, Thessaloniki, Greece
来源：
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL | 2010年 / 95卷
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
1856
引用
收藏
页码：717 / 717
页数：1
相关论文
共 50 条
  • [31] Compound heterozygosity for Hb E and Hb Lepore-Hollandia in India; First report and potential diagnostic pitfalls
    Edison, ES
    Shaji, RV
    Srivastava, A
    Chandy, M
    HEMOGLOBIN, 2005, 29 (03) : 221 - 224
  • [32] COMPOUND HETEROZYGOSITY FOR HAEMOGLOBIN ADANA AND A-THALASSAEMIA IN GREECE. CLINICAL PHENOTYPE AND GENETIC COUNSELING
    Theodoridou, S.
    Teli, A.
    Yfanti, E.
    Vyzantiadis, T. -A.
    Economou, M.
    HAEMATOLOGICA, 2017, 102 : 870 - 870
  • [33] Compound heterozygosity for triplicated α-globin gene and (- -SEA) α-globin gene deletion:: Implication for thalassaemia screening
    Ma, SK
    Chan, AYY
    Chan, LC
    Chui, DHK
    Waye, JS
    BRITISH JOURNAL OF HAEMATOLOGY, 2000, 110 (02) : 498 - 499
  • [34] Lipaemic serum in Hb E-Beta thalassaemia major: A rare case of hypertriglyceridaemia thalassaemia syndrome
    Mohd Kasim, Noor Alicezah
    Mohd Nor, Noor Shafina
    Wen, Mang Teen
    Syed Kamaruddin, Sharifah Khairul Atikah
    Sheikh Abdul Kadir, Siti Hamimah
    MALAYSIAN JOURNAL OF PATHOLOGY, 2023, 45 (02) : 293 - 296
  • [35] A Case Report of Compound Heterozygosity for β0/β+-Thalassemia Resulting from under Diagnosed β-Thalassemia Found in a Hb A'2 Sample
    Intasai, Nutjeera
    Phasit, Ampai
    Panyasai, Sitthichai
    Pornprasert, Sakorn
    HEMOGLOBIN, 2019, 43 (01) : 63 - 65
  • [36] Compound heterozygote states for Hb C/Hb Malay and Hb C/Hb E in pregnancy: A molecular and hematological analysis
    Fucharoen, S
    Fucharoen, G
    Sanchaisuriya, K
    Surapot, S
    BLOOD CELLS MOLECULES AND DISEASES, 2005, 35 (02) : 196 - 200
  • [37] Hematological characteristics and effective screening for compound heterozygosity for Hb Constant Spring and deletional α+-thalassemia
    Uaprasert, Noppacharn
    Rojnuckarin, Ponlapat
    Settapiboon, Rung
    Amornsiriwat, Supaporn
    Sutcharitchan, Pranee
    AMERICAN JOURNAL OF HEMATOLOGY, 2011, 86 (07) : 615 - 617
  • [38] Compound heterozygosity for Hb Tacoma [β30(B12)Arg→Ser] and β+-thalassemia
    Landin, B
    Alvelius, G
    Rai, DK
    Elinder, G
    HEMOGLOBIN, 2000, 24 (03) : 253 - 257
  • [39] A case of late diagnosis of compound heterozygosity for Hb Adana (HBA2:c.179G>A) in trans to an α plus - thalassemia deletion: guilty or innocent
    Tampaki, A.
    Theodoridou, S.
    Apostolou, Ch
    Delaki, E. E.
    Vlachaki, E.
    HIPPOKRATIA, 2020, 24 (01) : 43 - 45
  • [40] HB S(C)-BETA+-THALASSAEMIA - DIFFERENT MUTATIONS ARE ASSOCIATED WITH DIFFERENT LEVELS OF NORMAL HB-A
    GONZALEZREDONDO, JM
    KUTLAR, F
    KUTLAR, A
    STOMING, TA
    DEPABLOS, JM
    KILINC, Y
    HUISMAN, THJ
    BRITISH JOURNAL OF HAEMATOLOGY, 1988, 70 (01) : 85 - 89
12345