Severe thalassemia syndrome caused by Hemoglobin Pak Num Po AEBart's disease: A hematological, molecular, and diagnostic aspects

被引：2
作者：
Singha, Kritsada [1 ]
Wiangnon, Surapon [2 ]
Fucharoen, Goonnapa [1 ]
Jetsrisuparb, Arunee [3 ]
Komwilaisak, Patcharee [3 ]
Fucharoen, Supan [1 ]
机构：
[1] Khon Kaen Univ, Fac Associated Med Sci, Med Diagnost Labs, Ctr Res & Dev, Khon Kaen, Thailand
[2] Mahasarakham Univ, Fac Med, Maha Sarakham, Thailand
[3] Khon Kaen Univ, Dept Pediat, Fac Med, Khon Kaen, Thailand
来源：
INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY | 2020年 / 42卷 / 04期
关键词：
PHENOTYPE; GENOTYPE; COHORT;
D O I：
10.1111/ijlh.13224
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：E173 / E176
页数：4
相关论文
共 10 条
[1]   Genetic heterogeneity of hemoglobin AEBart's disease: A large cohort data from a single referral center in northeast Thailand [J].
Chaibunruang, Attawut ;
Karnpean, Rossarin ;
Fucharoen, Goonnapa ;
Fucharoen, Supan .
BLOOD CELLS MOLECULES AND DISEASES, 2014, 52 (04) :176-180
[2]   NPS@:: Network Protein Sequence Analysis [J].
Combet, C ;
Blanchet, C ;
Geourjon, C ;
Deléage, G .
TRENDS IN BIOCHEMICAL SCIENCES, 2000, 25 (03) :147-150
[3]   Molecular basis of α-thalassemia [J].
Farashi, Samaneh ;
Harteveld, Cornelis L. .
BLOOD CELLS MOLECULES AND DISEASES, 2018, 70 :43-53
[4]  
Fucharoen S, 1988, BIRTH DEFECTS ORIG A, V23, P327
[5]   Phenotype and Genotype in a Cohort of 312 Adult Patients with Nontransfusion-Dependent Thalassemia in Northeast Thailand [J].
Prayalaw, Patcharawadee ;
Teawtrakul, Nattiya ;
Jetsrisuparb, Arunee ;
Pongudom, Saranya ;
Fucharoen, Goonnapa ;
Fucharoen, Supan .
ACTA HAEMATOLOGICA, 2016, 135 (01) :15-20
[6]   Variable Genotype-Phenotype Correlations in Patients With a Rare Nondeletional α-thalassemia; Hb Pak Num Po ( HBA1: c. 396_ 397insT) [J].
Sanpakit, Kleebsabai ;
Viprakasit, Vip .
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2014, 36 (03) :E185-E189
[7]   Dominant β-thalassaemia with unusually high Hb A2 and Hb F caused by βCD121(-G) (HBB:c.364delG) in exon 3 of β-globin gene [J].
Singha, Kritsada ;
Karnpean, Rossarin ;
Fucharoen, Goonnapa ;
Fucharoen, Supan .
JOURNAL OF CLINICAL PATHOLOGY, 2020, 73 (08) :511-513
[8]   Molecular basis of Hb H and AEBart's diseases in the Lao People's Democratic Republic [J].
Singha, Kritsada ;
Srivorakun, Hataichanok ;
Fucharoen, Goonnapa ;
Fucharoen, Supan .
INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY, 2020, 42 (01) :23-27
[9]   Co-inheritance of Hb Pak Num Po, a novel α1 gene mutation, and α0 thalassemia associated with transfusion-dependent Hb H disease [J].
Viprakasit, V ;
Tanphaichitr, VS ;
Veerakul, G ;
Chinchang, W ;
Petrarat, S ;
Pung-Amritt, P ;
Iggs, DRH .
AMERICAN JOURNAL OF HEMATOLOGY, 2004, 75 (03) :157-163
[10]   Prevention of severe thalassemia in northeast Thailand: 16 years of experience at a single university center [J].
Yamsri, Supawadee ;
Sanchaisuriya, Kanokwan ;
Fucharoen, Goonnapa ;
Sae-ung, Nattaya ;
Ratanasiri, Thawalwong ;
Fucharoen, Supan .
PRENATAL DIAGNOSIS, 2010, 30 (06) :540-546
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