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Constitutional mismatch repair deficiency presenting in childhood as three simultaneous malignancies

  • Andrew W. Walter
  • , Sara Ennis
  • , Hunter Best
  • , Cecily P. Vaughn
  • , Jeffrey J. Swensen
  • , Amanda Openshaw
  • , Karen W. Gripp
  • Alfred I. duPont Hospital for Children
  • University of Utah

Producción científica › revisión exhaustiva

13 Citas (Scopus)

Resumen

A 13-year-old child presented with three simultaneous malignancies: glioblastoma multiforme, Burkitt lymphoma, and colonic adenocarcinoma. She was treated for her diseases without success and died 8 months after presentation. Genetic analysis revealed a homozygous mutation in the PMS2 gene, consistent with constitutional mismatch repair deficiency. Her siblings and parents were screened: three of four siblings and both parents were heterozygous for this mutation; the fourth sibling did not have the <!--mutation. Pediatr Blood Cancer 2013;60:E135-E136.

Idioma originalEnglish
Páginas (desde-hasta)E135-E136
PublicaciónPediatric Blood and Cancer
Volumen60
N.º11
DOI
EstadoPublished - nov 2013

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