Article
Hearing impairment caused by mutations in two different genes responsible for nonsyndromic and syndromic hearing loss within a single family.
Journal of applied genetics - 1 Feb 2018
Niepokój Katarzyna, Rygiel Agnieszka M, Jurczak Piotr, Kujko Aleksandra A, Śniegórska Dominika, Sawicka Justyna, Grabarczyk Alicja, Bal Jerzy, Wertheim-Tysarowska Katarzyna
Abstract excerpt
Usher syndrome is rare genetic disorder impairing two human senses, hearing and vision, with the characteristic late onset of vision loss. This syndrome is divided into three types. In all cases, the vision loss is postlingual, while loss of hearing is usually prelingual. The vestibular functions may also be disturbed in Usher type 1 and sometimes in type 3. Vestibular areflexia is helpful in making a proper...
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