x

Search for a diagnostic test

* (*) mandatory field

Biochemical diagnosis of Congenital Disorder of Glycosylation, type Ia (Analyte: Phosphomannomutase)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 11/11/2009
  • Laboratorium Enzymdiagnostiek
  • Afdeling Klinische Genetica - Sectie Genetische Metabole Ziekten
  • Erasmus MC, Faculteitsgebouw
  • Dr. Molewaterplein 50
  • 3015 GE ROTTERDAM
  • NETHERLANDS
  • Director of laboratory : Dr F.W. [Frans] VERHEIJEN
  • More information
  • Phone : 31 (0)10 7043212
  • Additional Phone : -
  • Fax : 31 (0)10 7043200
  • Website
  • Contact
Last update: November 2009

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Biochemical genetics
Analyte / Enzyme assay
-

List of diseases and genes

List of diseases tested (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.