Audiologic Features of Norrie Disease
Date
Authors
Halpin, Chris
Owen, Grace
Gutiérrez Espeleta, Gustavo A.
Sims, Katherine B.
Rehm, Heidi L.
Journal Title
Journal ISSN
Volume Title
Publisher
Ann Otol Rhinol Laryngol 114 (7) p. 533-538
Abstract
Objectives: Norrie disease is an X-linked recessive disorder in which patients are born blind and develop sensory hearing
loss in adolescence. The hearing loss associated with Norrie disease has been shown in a genetically altered knockout
mouse to involve dysfunction of the stria vascularis; most other structures are preserved until the later stages of the
disease. The objective of this study was to characterize the audiologic phenotype of Nark disease for comparison with
the pathophysiologic mechanism.
Methods: The design combined two series of clinical audiologic evaluations, with special attention to speech intelligibility.
Results: The audiologic results for 12 affected individuals and 10 carriers show that patients with Norrie disease retain
high speech intelligibility scores even when the threshold loss is severe.
Conclusions: The cochlear mechanism — failure of the stria vascularis — accounts for some of the higher values in the
wide distribution of speech scores in cases with similar pure tone and iograms.
Description
Artículo científico -- Instituto de Investigaciones en Salud. 2005
Keywords
audiometry, stria vascularis, speech intelligibility, NDP gene, Norrie disease, Human genetics, Genética humana