Hb Brugg [HBA1:c.63C>A]: Report of an Ultra-Rare Variant Hemoglobin and Its Co-inheritance with Hb D-Punjab

被引：2
|
作者：
Sharma, Abhishek [1 ]
Das, Reena [1 ]
Khadwal, Alka Rani [2 ]
Hira, Jasbir Kaur [1 ]
Chhabra, Sanjeev [1 ]
Kumar, Verinder [1 ]
Sharma, Prashant [1 ]
机构：
[1] Postgrad Inst Med Educ & Res, Dept Hematol, Level 5,Res Block A,Sect 12, Chandigarh, India
[2] Postgrad Inst Med Educ & Res, Dept Internal Med, Adult Clin Hematol & BMT Unit, Chandigarh, India
来源：
INDIAN JOURNAL OF HEMATOLOGY AND BLOOD TRANSFUSION | 2021年 / 37卷 / 02期
关键词：
D O I：
10.1007/s12288-020-01331-7
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：326 / 328
页数：3
相关论文
共 39 条
  • [1] Hb Brugg [HBA1:c.63C>A]: Report of an Ultra-Rare Variant Hemoglobin and Its Co-inheritance with Hb D-Punjab
    Abhishek Sharma
    Reena Das
    Alka Rani Khadwal
    Jasbir Kaur Hira
    Sanjeev Chhabra
    Verinder Kumar
    Prashant Sharma
    Indian Journal of Hematology and Blood Transfusion, 2021, 37 : 326 - 328
  • [2] A Novel Case of Co-Inheritance of Rare Hemoglobin Variant; Hb Rancho Mirage [βCd 143 (CAC→GAC) His→Asp] with Hb D-Punjab
    Al Zaabi, Eiman A.
    Mahmoud, Amira
    Baysal, Erol
    Spence, David G.
    BLOOD, 2012, 120 (21)
  • [3] Hb Memphis [HBA2: c.70G>C (or HBA1)] in a Turkish Child: A Case Report and Comparison to Hb Q-Thailand (HBA1: c.223G>C)
    Lubrano, Lauren
    Donnelly, Michael J.
    Sandler, Gerald
    Hoyer, James D.
    Swanson, Kenneth C.
    Dawson, D. Brian
    Oliveira, Jennifer L.
    HEMOGLOBIN, 2014, 38 (02) : 137 - 141
  • [4] A New Hemoglobin Variant, Hb Natal (HBA1: c.423C>A), Found in a Greek Family
    Efstathiou, Anna
    Boutou, Effrossyni
    Teli, Aikaterini
    Drikos, Ioannis
    Balassopoulou, Angeliki
    Theodoridou, Stamatia
    HEMOGLOBIN, 2022, 46 (02) : 132 - 136
  • [5] Asymptomatic Co-Inheritance of Hb Leiden (HBB:c.22_24delGAG), Hb Q-Thailand (HBA1:c.223G > C) and Deletional Alpha Thalassemia in a Young Chinese Male
    Ren, Tianfeng
    Liang, Liang
    Li, Youqiong
    INDIAN JOURNAL OF HEMATOLOGY AND BLOOD TRANSFUSION, 2025, 41 (01) : 191 - 193
  • [6] Fifteen Cases of Hb J-Meerut: The Rare Association with Hb E and/or HBA1: c.-24C>G (or HBA2) Variants
    Khalil, Mohamed S. M.
    Timbs, Adele T.
    Henderson, Shirley J.
    Schuh, Anna
    Old, John M.
    HEMOGLOBIN, 2020, 44 (05) : 364 - 367
  • [7] Hb Jishui [HBA1: c.225C>G, Codon 74 (GAC>GAG), Asp→Glu]: A Novel α Chain Hemoglobin Variant Detected During Hb A1c Measurement
    Xie, Weijie
    Zheng, Huiqi
    Xu, Anping
    Ji, Ling
    HEMOGLOBIN, 2021, 45 (04) : 259 - 261
  • [8] Hb Hubei [114(GH2)ProHis, HBA1: c.344C>A]: A Novel Hemoglobin Variant of the 1-Globin Chain
    Xu, An-Ping
    Li, Jie
    Chen, Wei-Dong
    Zhou, Yu
    Ji, Ling
    HEMOGLOBIN, 2018, 42 (03) : 206 - 208
  • [9] First Report of Association Between Rare -Thalassemia Mutation (HBA1: c.298A>T) and Hb Fontainebleau (HBA2: c.64G>C)
    Ghadami, Elham
    Tamaddoni, Ahmad
    Sedaghat, Sadegh
    Tabaripour, Reza
    Baboli, Hadis Pourreza
    Akhavan-Niaki, Haleh
    INDIAN JOURNAL OF CLINICAL BIOCHEMISTRY, 2019, 34 (01) : 115 - 117
  • [10] Severe Hb H Disease Caused by Hb Zurich-Albisrieden (HBA1: c.178G>C): Another Case Report
    Wu, Shao-Min
    Huang, Su-Ran
    Li, Chan
    Chen, Gui-Lan
    Li, Dong-Zhi
    HEMOGLOBIN, 2022, 46 (06) : 341 - 343
1234