Orphanet: Diagnostik des Dravet Syndroms SCN1A Gen: Sequenzierung, MLPA
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Diagnosis of Dravet syndrome (SCN1A genes: sequencing, MLPA)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 27/03/2012
  • Gemeinschaftspraxis Dr. Prager / Dr. Junge / Dr. Hennig / Dr. Linné / Dr. Fink
  • MVZ Mitteldeutscher Praxisverbund Humangenetik GmbH
  • Friedrichstrasse 38 - 40
  • 01067 DRESDEN
  • GERMANY
  • Director of laboratory : -
  • More information
  • Phone : 49 (0)351 49278900
  • Additional Phone : 49 (0)351 49278950
  • Fax : 49 (0)351 49278955
  • Website
  • Contact
Last update: March 2012

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
Sanger sequencing
Deletion / Duplication analysis
MLPA based techniques

List of diseases and genes

List of diseases tested (1)
List of genes tested (including panels) (1)
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.