Williams-Beuren Syndrome and Burkitt Leukemia.

doi:10.1097/MPH.0b013e318270672f

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Article

Williams-Beuren Syndrome and Burkitt Leukemia.

Journal of pediatric hematology/oncology - 1 Jan 2013

Zhukova Nataliya, Naqvi Ahmed

Abstract excerpt

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...

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Share to Burkitt Lymphoma
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Share to Chromosomes, Human, Pair 7
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Identifiers

PMID: 23018576
DOI: 10.1097/MPH.0b013e318270672f

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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