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Ordering Genetic Hearing Loss Testing |
Ordering Genetic Renal Panel Testing |
Ordering Complement Functional Testing |
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. |
Genetic Renal Panel screens patients diagnosed with thrombotic microangiopathies and C3 glomerulopathy. The next-generation sequencing panel includes analysis of 13 genes for single nucleotide variants as well as MLPA, which identifies copy-number variations in the CFH-CFHR5 genomic region. | Comprehensive complement testing includes quantitating complement proteins and their cleavage products, measuring complement activity, and screening for autoantibodies. |
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MORL Employment Opportunities
Preliminary enquiries, together with a CV, should be sent to: morl@uiowa.edu |
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Conferences2023 Family C3G Conference
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What does it mean to get your testing done at the MORL?
- 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.