Orphanet: Diagnostic du syndrome ICCA g�ne PRRT2
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Diagnosis of ICCA syndrome (PRRT2 gene)

  • Laboratoire de Gntique Molculaire Mdicale
  • Centre de biologie humaine (CBH)
  • CHU Amiens-Picardie - Site Sud
  • 1 Rond Point du Professeur Christian Cabrol
  • 80054 AMIENS CEDEX 1
  • FRANCE
  • Director of laboratory : Pr Loc GARON
  • More information
  • Phone : 33 (0)3 22 08 71 10
  • Additional Phone : -
  • Fax : 33 (0)3 22 08 71 09
Last update: February 2019

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Mutation scanning/screening and sequence analysis of selected exons
Sanger sequencing

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.