Deafness, autosomal dominant 3B
Analysis ID 188
Analysis location “GENESIS” Centre for Medical Genetics
Diagnosed illness Deafness, autosomal dominant 3B
OMIM #612643
Clinical information Isolated, non-syndromic hearing loss is a disorder in which deafness is not associated with other accompanying features. In many cases non-syndromic deafness has genetic origin and can be caused by mutation in the GJB6 gene.
Type of analysis Molecular
Type of biological material 5 ml of peripheral blood collected in an ETDA tube; DNA sample
Analyzed genes GJB6
Analysis description Sequencing of the entire coding region of the GJB6 gene
Analysis indication Deafness
Analysis time 3 - 4 weeks
Refund Yes
CGM laboratory name Laboratory for Molecular Genetics