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Constitutional and somatic deletions of the Williams-Beuren syndrome critical region in Non-Hodgkin Lymphoma

Guenat, David (author)
Quentin, Samuel (author)
Rizzari, Carmelo (author)
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Lundin, Catarina (author)
Lund University,Lunds universitet,Avdelningen för klinisk genetik,Institutionen för laboratoriemedicin,Medicinska fakulteten,Division of Clinical Genetics,Department of Laboratory Medicine,Faculty of Medicine
Coliva, Tiziana (author)
Edery, Patrick (author)
Fryssira, Helen (author)
Bermont, Laurent (author)
Ferrand, Christophe (author)
Soulier, Jean (author)
Borg, Christophe (author)
Rohrlich, Pierre-Simon (author)
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 (creator_code:org_t)
2014-11-07
2014
English.
In: Journal of Hematology & Oncology. - : Springer Science and Business Media LLC. - 1756-8722. ; 7
  • Journal article (other academic/artistic)
Abstract Subject headings
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  • Here, we report and investigate the genomic alterations of two novel cases of Non-Hodgkin Lymphoma (NHL) in children with Williams-Beuren syndrome (WBS), a multisystem disorder caused by 7q11.23 hemizygous deletion. Additionally, we report the case of a child with NHL and a somatic 7q11.23 deletion. Although the WBS critical region has not yet been identified as a susceptibility locus in NHL, it harbors a number of genes involved in DNA repair. The high proportion of pediatric NHL reported in WBS is intriguing. Therefore, the role of haploinsufficiency of genes located at 7q11.23 in lymphomagenesis deserves to be investigated.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Medicinsk genetik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Medical Genetics (hsv//eng)

Keyword

Williams-Beuren syndrome
Non-Hodgkin Lymphoma
7q11.23
Cancer
predisposition
DNA repair

Publication and Content Type

art (subject category)
vet (subject category)

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