Literature DB >> 18413893

{beta}-thalassemia major evolution from {beta}-thalassemia minor is associated with paternal uniparental isodisomy of chromosome 11p15.

Jan-Gowth Chang1, Wen-Chan Tsai, Inn-Wen Chong, Chao-Sung Chang, Chyi-Chang Lin, Ta-Chih Liu.   

Abstract

beta-thalassemia major can be caused by homozygosity or compound heterozygosity for beta-globin gene mutations (HBB gene). Most cases are inherited from parents who both have diseased alleles of the HBB gene. We report a patient with late-onset beta-thalassemia major that evolved from beta-thalassemia minor in which only one of her parents had the diseased HBB gene. To study the cause of beta-thalassemia major in this patient, we performed the 100K single nucleotide polymorphism genotyping assay, fluorescence in situ hybridization, and DNA methylation analysis of the imprinting genes near the HBB gene. The results showed a loss of heterozygosity in the region of chromosome 11p14.3 to 11p15.5, which perfectly matched one allele of her father. Our study demonstrates that paternal uniparental isodisomy of chromosomal 11p15.5 is associated with the beta-thalassemia major in this patient. Key words: beta-thalassemia major, uniparental isodisomy, mosaicism.

Entities:  

Mesh:

Year:  2008        PMID: 18413893     DOI: 10.3324/haematol.12195

Source DB:  PubMed          Journal:  Haematologica        ISSN: 0390-6078            Impact factor:   9.941


  8 in total

1.  Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locus.

Authors:  Hannah Bogardus; Vincent P Schulz; Yelena Maksimova; Barbara A Miller; Peining Li; Bernard G Forget; Patrick G Gallagher
Journal:  Haematologica       Date:  2014-06-03       Impact factor: 9.941

Review 2.  Molecular basis of β thalassemia and potential therapeutic targets.

Authors:  Swee Lay Thein
Journal:  Blood Cells Mol Dis       Date:  2017-06-20       Impact factor: 3.039

3.  Rapid Screening for Deleted Form of β-thalassemia by Real-Time Quantitative PCR.

Authors:  Liang-Yin Ke; Jan-Gowth Chang; Chao-Sung Chang; Li-Ling Hsieh; Ta-Chih Liu
Journal:  J Clin Lab Anal       Date:  2016-08-16       Impact factor: 2.352

4.  Mosaic segmental uniparental isodisomy and progressive clonal selection: a common mechanism of late onset β-thalassemia major.

Authors:  Cornelis L Harteveld; Chiara Refaldi; Antonino Giambona; Claudia A L Ruivenkamp; Mariëtte J V Hoffer; Jeroen Pijpe; Peter De Knijff; Caterina Borgna-Pignatti; Aurelio Maggio; Maria D Cappellini; Piero C Giordano
Journal:  Haematologica       Date:  2012-09-14       Impact factor: 9.941

Review 5.  The molecular basis of β-thalassemia.

Authors:  Swee Lay Thein
Journal:  Cold Spring Harb Perspect Med       Date:  2013-05-01       Impact factor: 6.915

6.  A Beckwith-Wiedemann syndrome case with de novo 24 Mb duplication of chromosome 11p15.5p14.3.

Authors:  Huling Jiang; Zepeng Ping; Jianguo Wang; Xiaodan Liu; Yuxia Jin; Suping Li; Chiyan Zhou; Pinghua Huang; Yi Jin; Ling Ai; Jie Chen
Journal:  Mol Cytogenet       Date:  2021-03-03       Impact factor: 2.009

Review 7.  The hemoglobinopathies, molecular disease mechanisms and diagnostics.

Authors:  Cornelis L Harteveld; Ahlem Achour; Sandra J G Arkesteijn; Jeanet Ter Huurne; Maaike Verschuren; Sharda Bhagwandien-Bisoen; Rianne Schaap; Linda Vijfhuizen; Hakima El Idrissi; Tamara T Koopmann
Journal:  Int J Lab Hematol       Date:  2022-09       Impact factor: 3.450

8.  β Thalassemia major due to acquired uniparental disomy in a previously healthy adolescent.

Authors:  Celeste Bento; Tabita M Maia; Jelena D Milosevic; Isabel M Carreira; Robert Kralovics; M Leticia Ribeiro
Journal:  Haematologica       Date:  2012-08-08       Impact factor: 9.941

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.