Literature DB >> 23018576

Williams-Beuren Syndrome and Burkitt Leukemia.

Nataliya Zhukova1, Ahmed Naqvi.   

Abstract

Williams-Beuren Syndrome (WBS) is associated with constitutional deletion of 7q11.23, which includes the elastin gene. Cytogenetic abnormalities of chromosome 7 are frequently described in several human malignancies. Here, we report Burkitt Leukemia in an 8-year-old boy with WBS. In this patient, constitutional deletion of chromosome 7q11.23 including BCL7B was confirmed. WBS may predispose patients to Burkitt Leukemia.

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Year:  2013        PMID: 23018576     DOI: 10.1097/MPH.0b013e318270672f

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN: 1077-4114            Impact factor:   1.289


  6 in total

1.  BCL7C suppresses ovarian cancer growth by inactivating mutant p53.

Authors:  Canhua Huang; Qian Hao; Getao Shi; Xiang Zhou; Yu Zhang
Journal:  J Mol Cell Biol       Date:  2021-05-07       Impact factor: 6.216

2.  Constitutional and somatic deletions of the Williams-Beuren syndrome critical region in non-Hodgkin lymphoma.

Authors:  David Guenat; Samuel Quentin; Carmelo Rizzari; Catarina Lundin; Tiziana Coliva; Patrick Edery; Helen Fryssira; Laurent Bermont; Christophe Ferrand; Jean Soulier; Christophe Borg; Pierre-Simon Rohrlich
Journal:  J Hematol Oncol       Date:  2014-11-07       Impact factor: 17.388

3.  The Tumor Suppressor BCL7B Functions in the Wnt Signaling Pathway.

Authors:  Tomoko Uehara; Eriko Kage-Nakadai; Sawako Yoshina; Rieko Imae; Shohei Mitani
Journal:  PLoS Genet       Date:  2015-01-08       Impact factor: 5.917

4.  Williams-Beuren Syndrome as a Potential Risk Factor for Burkitt Lymphoma.

Authors:  Ryo Kimura; Yuko Ishii; Kiyotaka Tomiwa; Tomonari Awaya; Masatoshi Nakata; Takeo Kato; Shin Okazaki; Toshio Heike; Masatoshi Hagiwara
Journal:  Front Genet       Date:  2018-09-04       Impact factor: 4.599

5.  Cognition in adults with Williams syndrome-A 20-year follow-up study.

Authors:  Oili Sauna-Aho; Nina Bjelogrlic-Laakso; Auli Sirén; Virpi Kangasmäki; Maria Arvio
Journal:  Mol Genet Genomic Med       Date:  2019-04-29       Impact factor: 2.183

Review 6.  Dental-craniofacial manifestation and treatment of rare diseases.

Authors:  En Luo; Hanghang Liu; Qiucheng Zhao; Bing Shi; Qianming Chen
Journal:  Int J Oral Sci       Date:  2019-02-20       Impact factor: 6.344

  6 in total

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