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  • Providing the most accurate clinically-driven interpretation of genetic variants in a timely manner Testing at MORL
  • Providing the most accurate clinically-driven interpretation of genetic variants in a timely manner Testing at MORL
  • Providing the most accurate clinically-driven interpretation of genetic variants in a timely manner Testing at MORL
  • Providing the most accurate clinically-driven interpretation of genetic variants in a timely manner Testing at MORL
  • Providing the most accurate clinically-driven interpretation of genetic variants in a timely manner Testing at MORL
OtoSCOPE TMA thumb complement testing

Genetic Hearing Loss

Genetic Renal Panel

Complement Tests
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.
Research Portal

aHUS Longitudinal Study

Conferences                     

2017 C3G Family Conference Flyer

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Helping to Make Lives Better (Videos)

The University of Iowa
285 Newton Rd., 5270 CBRB
Iowa City, IA 52242
Phone: 319-335-6623
Fax: 319-353-5869
Email: morl@uiowa.edu

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What does it mean to get your testing done at the MORL?

 OtoSCOPE group3

  • Your results are discussed at a multidisciplinary meeting.
  • Your testing is done in the Clinical Division of the MORL by scientists who lead the world in the human genetics of deafness and complement-mediated renal diseases.
  • Your testing is the most comprehensive clinical testing available