Orphanet: Diagnostik des Lynch Syndroms MLH1, MSH2, MSH6, PMS2 und EPCAM Gen
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Diagnosis of Lynch syndrome (MLH1, MSH2, MSH6, PMS2, and EPCAM gene)

  • Zentrum für Medizinische Genetik
  • Hanusch Krankenhaus
  • Heinrich-Collin-Straße 30
  • 1140 WIEN
  • AUSTRIA
  • Director of laboratory : -
  • More information
  • Phone : +43 (0)1 910 21 84580
  • Additional Phone : -
  • Fax : -
  • Website
  • Contact
Last update: September 2019

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
Sanger sequencing
Sequence analysis: entire coding region
NGS sequencing (except WES)

List of diseases and genes

List of diseases tested (1)
List of genes tested (including panels) (5)

Quality management

EQA
 EQA

EQA scheme(s) organized by EMQN

HNPCC (Hereditary non-polyposis colon cancer)
2019

EQA scheme(s) organized by GenQA

Lynch syndrome
2018
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.