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complement testing

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.

MORL Employment Opportunities

Preliminary enquiries, together with a CV, should be sent to: morl@uiowa.edu

Research at MORL


2024 Family C3G Conference
October 4-5, 2024

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.