Orphanet: Molecular Diagnosis of Progressive Myoclonic Epilepsy NGS Panel 12 genes

Search for a diagnostic test

* (*) mandatory field

Molecular Diagnosis of Progressive Myoclonic Epilepsy NGS Panel (12 genes)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 09/06/2016
  • Molecular Genetics Laboratory
  • Department of Pathology and Laboratory Medicine
  • London Health Sciences Centre
  • 800 Commissioners Rd. East
  • Director of laboratory : Dr Bekim SADIKOVIC
  • More information
  • Phone : 1 (519) 685-8122
  • Additional Phone : -
  • Fax : 1 (519) 685-8279
  • Website
Last update: June 2016

Responsible of diagnostic test


Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
NGS sequencing (except WES)
Deletion / Duplication analysis
NGS sequencing (except WES)

List of diseases and genes

List of genes tested (including panels) (12)

Additional information

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.