|OtoSCOPE provides comprehensive genetic testing for all genes implicated in non-syndromic hearing loss and many types of syndromic hearing loss. An Usher Syndrome Panel is also available.||The Genetic Renal Panel tests for genetic causes of TMA (aHUS and TTP) and C3G (DDD and C3GN). The Panel includes analysis for complex genomic rearrangements of the CFHR region.||Comprehensive complement testing includes quantitating complement proteins and their cleavage products, measuring complement activity, and screening for autoantibodies.|
- Your results are discussed at a multidisciplinary meeting.
- Your testing is performed in the Clinical Division of the MORL by scientists who lead the world in the human genetics of deafness and complement-mediated renal diseases.
- Our testing is the most comprehensive clinical testing available.