Orphanet: Biochemicka diagnostika peroxizomovych ochoreni analyt: mastne kyseliny s velmi dlhym retazcom, kyseliny pristanovej, fytanovej, pipekolovej a plazmalogenov

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Biochemical diagnosis of peroxisomal disorders (analyte: very long chain fatty acids, pristanic acid, phytanic acid, pipecolic acid, plasmalogens)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 12/08/2013
  • Department of Molecular and Biochemical Genetics
  • Institute of Medical Biology, Genetics and Clinical Genetics, Faculty of Medicine of Comenius University, University Hospital
  • University Hospital Bratislava - Stare mesto
  • Mickiewiczova 13
  • 813 69 BRATISLAVA
  • Director of laboratory : Dr Jan CHANDOGA
  • More information
  • Phone : 00421257290192
  • Additional Phone : 00421257290244
  • Fax : -
  • Website
  • Contact
Last update: August 2013

Responsible of diagnostic test


Post-natal diagnosis

Technical procedure(s)

Biochemical genetics
Analyte / Enzyme assay

List of diseases and genes

List of diseases tested (1)
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