5p13 microduplication syndrome: A new case and better clinical definition of the syndrome

Francesca Novara, Enrico Alfei, Stefano D'Arrigo, Chiara Pantaleoni, Silvana Beri, Valentina Achille, Francesca L. Sciacca, Roberto Giorda, Orsetta Zuffardi, Roberto Ciccone

Research output: Contribution to journalArticle

Abstract

Chromosome 5p13 duplication syndrome (OMIM #. 613174), a contiguous gene syndrome involving duplication of several genes on chromosome 5p13 including NIPBL (OMIM 608667), has been described in rare patients with developmental delay and learning disability, behavioral problems and peculiar facial dysmorphisms. 5p13 duplications described so far present with variable sizes, from 0.25 to 13.6 Mb, and contain a variable number of genes. Here we report another patient with 5p13 duplication syndrome including NIPBL gene only. Proband's phenotype overlapped that reported in patients with 5p13 microduplication syndrome and especially that of subjects with smaller duplications. Moreover, we better define genotype-phenotype relationship associated with this duplication and confirmed that NIPBL was likely the major dosage sensitive gene for the 5p13 microduplication phenotype.

Original languageEnglish
Pages (from-to)54-58
Number of pages5
JournalEuropean Journal of Medical Genetics
Volume56
Issue number1
DOIs
Publication statusPublished - Jan 2013

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Keywords

  • 5p13 microduplication syndrome
  • Array-CGH
  • NIPBL

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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