MORL: A Clinical Revolution - At the Forefront of Precision Medicine for Hearing Impairment  (video)
MORL: The Cutting Edge of Research - Revolutionizing Genetic Research for Hearing Loss  (video)
Always the most comprehensive resource, the MORL expands clinical MLPA, ADAMTS-13 and Classical Pathway Testing. Click PDF iconhere for details.
OtoSCOPE
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complement testing

Genetic Hearing Loss

Genetic Renal Panel

Complement Tests

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.
Research Portal

 

Conferences                     

2017 C3G Family Conference

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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

Full Testing Menu

 

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

 

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  • 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