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Array based CGH and FISH fail to confirm duplication of 8p22-p23.1 in association with Kabuki syndrome
  1. J D Hoffman1,
  2. Y Zhang1,
  3. J Greshock2,
  4. K L Ciprero1,
  5. B S Emanuel1,
  6. E H Zackai1,
  7. B L Weber2,
  8. J E Ming1
  1. 1Division of Human Genetics, Department of Pediatrics, The Children’s Hospital of Philadelphia and The University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA
  2. 2Abramson Family Cancer Research Institute, The University of Pennsylvania
  1. Correspondence to:
 Dr Jeffrey E Ming
 The Children’s Hospital of Philadelphia, Abramson Research Building, Room 1002, 3615 Civic Center Boulevard, Philadelphia, PA 19104, USA; jemingmail.med.upenn.edu

Abstract

Background: Kabuki (Niikawa–Kuroki) syndrome comprises a characteristic facial appearance, cleft palate, congenital heart disease, and developmental delay. Various cytogenetically visible chromosomal rearrangements have been reported in single cases, but the molecular genetic basis of the condition has not been established. A recent report described a duplication of 8p22–p23.1 in 13/13 patients.

Objective: To determine the frequency of an 8p duplication in a cohort of patients with Kabuki syndrome.

Methods: An 8p duplication was sought using two independent methods—array based comparative genomic hybridisation (aCGH) and fluorescence in situ hybridisation (FISH)—in 15 patients with a definitive clinical diagnosis of Kabuki syndrome.

Results: No evidence for a duplication of 8p was obtained by FISH or aCGH in any of the 15 patients.

Conclusions: 8p22–p23.1 duplication may not be a common mechanism for Kabuki syndrome. Another genetic abnormality may be responsible for the aetiology in many patients.

  • aCGH, array based comparative genomic hybridisation
  • BAC, bacterial artificial chromosome
  • FISH, fluorescence in situ hybridisation
  • Kabuki syndrome
  • FISH
  • array based comparative genomic hybridisation

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Footnotes

  • Competing interests: none declared