Optimizing the molecular diagnosis of CDKL5 gene-related epileptic encephalopathy in boys

Davide Mei, Francesca Darra, Carmen Barba, Carla Marini, Elena Fontana, Laura Chiti, Elena Parrini, Bernardo Dalla Bernardina, Renzo Guerrini

Research output: Contribution to journalArticlepeer-review

Abstract

Objective: Mutations involving the cyclin-dependent kinase-like 5 (CDKL5) gene cause an early onset epileptic encephalopathy (EE) with severe neurologic impairment and a skewed 12:1 female-to-male ratio. To date, 18 mutations have been described in boys. We analyzed our cohort of boys with early onset EE to assess the diagnostic yield of our molecular approach. Methods: We studied 74 boys who presented early onset severe seizures, including infantile spasms and developmental delay, in the setting of EE, using Sanger sequencing, next-generation sequencing (NGS) and multiplex ligation-dependent probe amplification (MLPA). Results: We identified alterations involving CDKL5 in four boys (5.4%) using NGS in one and MLPA in three. Three of four mutations were indicative of somatic mosaicism. Significance: CDKL5 gene mutations accounted for 5.4% of boys with early onset EE. Somatic mosaic mutations might be even more represented than germline mutations, probably because their less deleterious effect enhances viability of the male embryo. The molecular approach used for CDKL5 screening remarkably influences the diagnostic yield in boys. Diagnosis is optimized by Sanger sequencing combined with arraybased methods or MLPA; alternatively, NGS targeted resequencing designed to also detect copy number alterations, may be performed.

Original languageEnglish
Pages (from-to)1748-1753
Number of pages6
JournalEpilepsia
Volume55
Issue number11
DOIs
Publication statusPublished - Nov 1 2014

Keywords

  • CDKL5
  • Epileptic encephalopathy
  • Mosaic
  • Mutation

ASJC Scopus subject areas

  • Clinical Neurology
  • Neurology
  • Medicine(all)

Fingerprint

Dive into the research topics of 'Optimizing the molecular diagnosis of CDKL5 gene-related epileptic encephalopathy in boys'. Together they form a unique fingerprint.

Cite this