Orphanet: Molecular diagnosis of hereditary glaucoma MYOC, OPTN, WDR36 genes: mutation screening CYP1B1: prenatal screening
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Molecular diagnosis of hereditary glaucoma (MYOC, OPTN, WDR36 genes: mutation screening ; CYP1B1: prenatal screening)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 05/12/2012
  • Phone : 45 43 260 100
  • Additional Phone : -
  • Fax : 45 43 431 130
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Last update: December 2012

Responsible of diagnostic test

Purpose(s)

Antenatal diagnosis

Technical procedure(s)

Molecular genetics
Mutation scanning/screening and sequence analysis of selected exons
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List of diseases and genes

List of diseases tested (1)
List of genes tested (including panels) (4)
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.