Literature DB >> 29161910

Characterization of a Large Novel α-Globin Gene Cluster Deletion Causing α0-Thalassemia in a Chinese Family.

Sheng He1, Qian Qin2, Peng Huang1, Shujie Zhang1, Shang Yi1, Li Lin1, Yangjin Zuo1, Qiuli Chen1, Jianping Deng2, Chenguang Zheng1, Biyan Chen1.   

Abstract

We report a large novel α-globin cluster deletion that we named - -PG (NG_000006.1: g.93628_542759del450131), in a Chinese family. This large deletion is approximately 450 kb long, spanning from upstream of the PolR3k gene at the 5' end to the RAB11FIP3 gene at the 3' end of chromosome 16p13.3. This deletion removes all the globin distal regulatory elements as well as the whole α-globin gene cluster. Patients with heterozygous - -PG/αα had red blood cell (RBC) indices consistent with α-thalassemia (α-thal) trait, but no apparent increase in a cancer tendency or mental disability, microcephaly, relative hypertelorism, unusual facies or genital anomalies.

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Keywords:  array comparative genomic hybridization (aCGH); multiplex ligation-dependent probe amplification (MLPA); α-Globin gene cluster; α-thalassemia (α-thal)

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Year:  2017        PMID: 29161910     DOI: 10.1080/03630269.2017.1366919

Source DB:  PubMed          Journal:  Hemoglobin        ISSN: 0363-0269            Impact factor:   0.849


  1 in total

1.  Characterisation of two unusual cases of haemoglobin Bart's hydrops foetalis caused by -SEA and large novel α-globin gene cluster deletions.

Authors:  Yunan Wang; Ying Xiong; Chang Liu; Jian Lu; Jicheng Wang; DanQing Qin; Ling Liu; Jing Wu; Xin Zhao; Liyuan Fang; Li Du; Aihua Yin
Journal:  J Int Med Res       Date:  2021-02       Impact factor: 1.671

  1 in total

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