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The University of Iowa285 Newton Rd., 5270 CBRB Iowa City, IA 52242Phone: 319-335-6623 Fax: 319-353-5869Email: email@example.com
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OtoSCOPE provides comprehensive genetic testing for all genes implicated in non-syndromic hearing loss, Usher syndrome, and Pendred syndrome. An Usher Syndrome Panel is also available.
The Genetic Renal Panel attempts to determine the genetic cause of patients diagnosed with TMAs (aHUS) or C3Gs (DDD/C3GN); in the past this required multiple tests, the Genetic Renal Panel accomplishes the same objectives with one.
The MORL offers unique and specific assays for several complement-mediated diseases (C3GN, DDD, aHUS) to define complement profiles as an aid to patient care.