CDKL5 variant in a boy with infantile epileptic encephalopathy: case report

Brain Dev. 2015 Apr;37(4):446-8. doi: 10.1016/j.braindev.2014.07.003. Epub 2014 Jul 29.

Abstract

A Chinese boy presented at 18 months with intractable epilepsy, developmental delay and autistic features. He had multiple seizure types, including absence, myoclonic seizures, limb spasm and tonic seizures. His seizures were finally controlled at 3 years of age with clonazepam and a short course of chloral hydrate incidentally given for his insomnia. Subsequently, he had improvement in his communication skills.

Result: A novel hemizygous missense variant (c.1649G>A; p.R550Q) in exon 12 of CDKL5 gene was detected for him, his asymptomatic mother and elder sister. His phenotype is less severe than other male cases.

Conclusion: We recommend screening CDKL5 for boys with pharmarco-resistant epilepsy and a trial of benzodiazepines for Infantile Epileptic Encephalopathy (IEE).

Keywords: Anti-epileptic drugs; Benzodiazepines; CDKL5-epileptic encephalopathy; Chloral hydrate; Infantile Epileptic Encephalopathy (IEE); Intractable epilepsy.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anticonvulsants / adverse effects
  • Anticonvulsants / therapeutic use
  • Asian People / genetics
  • Autism Spectrum Disorder / diagnosis
  • Autism Spectrum Disorder / genetics*
  • Autism Spectrum Disorder / physiopathology
  • Benzodiazepines / adverse effects
  • Benzodiazepines / therapeutic use
  • China
  • Developmental Disabilities / diagnosis
  • Developmental Disabilities / genetics*
  • Developmental Disabilities / physiopathology
  • Diagnosis, Differential
  • Drug Resistance / genetics
  • Epilepsy / diagnosis
  • Epilepsy / drug therapy
  • Epilepsy / genetics*
  • Epilepsy / physiopathology
  • Genetic Variation
  • Humans
  • Infant
  • Male
  • Mutation, Missense
  • Protein Serine-Threonine Kinases / genetics*
  • Seizures / diagnosis
  • Seizures / drug therapy
  • Seizures / genetics
  • Seizures / physiopathology

Substances

  • Anticonvulsants
  • Benzodiazepines
  • Protein Serine-Threonine Kinases
  • CDKL5 protein, human