University of Hertfordshire

  • Eirini Tsoutsou
  • Maria Tzetis
  • Krinio Giannikou
  • Maria Braoudaki
  • Anastasis Mitrakos
  • Stella Amenta
  • Nikoletta Selenti
  • Emmanouil Kanavakis
  • Dimitrios Zafeiriou
  • Sophia Kitsiou-Tzeli
  • Helena Fryssira
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Original languageEnglish
Pages (from-to)253-260
Number of pages8
JournalPediatric research
Volume82
Issue2
DOIs
Publication statusPublished - 24 May 2017

Abstract

Backround: Microcephaly can either be isolated or it may coexist with other neurological entities and/or multiple congenital anomalies, known as syndromic microcephaly. Although many syndromic cases can be classified based on the characteristic phenotype, some others remain uncertain and require further investigation. The present study describes the application of array-comparative genomic hybridization (array-CGH) as a diagnostic tool for the study of patients with clinically unknown syndromic microcephaly. Methods: From a cohort of 210 unrelated patients referred with syndromic microcephaly, we applied array-CGH analysis in 53 undiagnosed cases. In all the 53 cases except one, previous standard karyotype was negative. High-resolution 4 × 180K and 1 × 244K Agilent arrays were used in this study. Results: In 25 out of the 53 patients with microcephaly among other phenotypic anomalies, array-CGH revealed copy number variations (CNVs) ranging in size between 15 kb and 31.6 Mb. The identified CNVs were definitely causal for microcephaly in 11/53, probably causal in 7/53, and not causal for microcephaly in 7/53 patients. Genes potentially contributing to brain deficit were revealed in 16/53 patients. Conclusions: Array-CGH contributes to the elucidation of undefined syndromic microcephalic cases by permitting the discovery of novel microdeletions and/or microduplications. It also allows a more precise genotype-phenotype correlation by the accurate definition of the breakpoints in the deleted/duplicated regions.

ID: 14882153