Orphanet: Diagnosi biochimica e molecolare della sindrome di Kearns Sayre analisi del DNA mitocondriale
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Biochemical and molecular diagnosis of Kearns-Sayre syndrome (mtDNA)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 14/09/2011
  • U.O. di Neurogenetica Molecolare
  • Dipartimento di Diagnostica e Tecnologia Applicata
  • Fondazione IRCCS Istituto Neurologico "C. Besta" - sede Bicocca
  • Via Libero Temolo 4
  • 20126 MILANO
  • ITALY
  • Director of laboratory : Dr Barbara GARAVAGLIA
  • More information
  • Phone : 39 02 23942604
  • Additional Phone : 39 02 23942618
  • Fax : 39 02 23942619
  • Website
  • Contact
Last update: September 2011

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
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Biochemical genetics
Analyte / Enzyme assay
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List of diseases and genes

List of diseases tested (1)
List of genes tested (including panels) (2)
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.