Hearing impairment caused by mutations in two different genes responsible for nonsyndromic and syndromic hearing loss within a single family

Abstract

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 diagnosis of the syndrome, but, often, the syndrome is misdiagnosed as a nonsyndromic hearing loss. Here, we present a Polish family with hearing loss, which was clinically classified as nonsyndromic. After excluding mutations in the DFNB1 locus, we implemented the next-generation sequencing method and revealed that hearing loss was syndromic and mutations in the USH2A gene indicate Usher syndrome. This research highlights the importance of molecular analysis in establishing a clinical diagnosis of congenital hearing loss.

Hearing reduction in patients with genetic diseases

“…При синдрома на Ушер се касае за учреждане на слуха и зрението. Съобщава се за семейство в Полша с първоначално диагностицирана загуба на слуха от несиндромен тип (13). След изключването на мутациите в локуса DFNB1 се провежда секвениране от следващо поколение и се доказват мутации в гена USH2A, идентифициращи синдрома на Ушер.…”