Orphanet: Diagnostik des kongenitalen Glaukoms Typ Peters Gene: CYP1B1, FOXC1, PAX6 und PITX2
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Diagnosis of Peters congenital glaucoma (CYP1B1, FOXC1, PAX6, PITX2 genes)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 30/06/2014
  • Labor Ingelheim mit Zentrum für Humangenetik
  • Bioscientia Institut für Medizinische Diagnostik GmbH
  • Konrad Adenauer Strasse 17
  • 55218 INGELHEIM AM RHEIN
  • GERMANY
  • Director of laboratory : Dr Mojgan DRASDO
  • More information
  • Phone : 49 (0)6132 781 411
  • Additional Phone : -
  • Fax : 49 (0)6132 781 194
  • Website
  • Contact
Last update: June 2014

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
Sanger sequencing

List of diseases and genes

List of diseases tested (1)
List of genes tested (including panels) (3)

Additional information

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.