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Molecular diagnosis of PEO, SANDO, Alpers syndrome, MNGIE (POLG, C10ORF2 genes)

  • Molecular laboratory, Department of Medical Genetics
  • Center of Medical Genetics
  • Centrum Medische Genetica - UZA
  • Prins Boudewijnlaan 43 Bus 6
  • 2650 ANTWERPEN-EDEGEM
  • BELGIUM
  • Director of laboratory : Pr Wim WUYTS
  • More information
  • Phone : +32 (0)3 275 97 74
  • Additional Phone : -
  • Fax : -
  • Website
Last update: May 2018

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
Sanger sequencing

Additional information

Quality management

EQA
 EQA

EQA scheme(s) organized by GenQA

Mitochondrial diseases (including POLG)
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.