{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,4]],"date-time":"2026-05-04T03:08:27Z","timestamp":1777864107000,"version":"3.51.4"},"reference-count":31,"publisher":"SAGE Publications","issue":"1","license":[{"start":{"date-parts":[[1987,1,1]],"date-time":"1987-01-01T00:00:00Z","timestamp":536457600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J R Soc Med"],"published-print":{"date-parts":[[1987,1]]},"abstract":"<jats:p>Seventeen patients with retinitis pigmentosa (RP) have been investigated audiologically. Of 9 found to have a significant hearing loss, 6 were examples of Usher's syndrome; these patients had a cochlear pattern of hearing loss. The other 3 were examples of Senior's syndrome, Kearne-Sayre syndrome and Lawrence-Moon-Biedle syndrome respectively. Two of these patients had absent stapedius reflexes. It is suggested that patients with different RP-deafness syndromes may have lesions in different parts of the auditory system.<\/jats:p>","DOI":"10.1177\/014107688708000108","type":"journal-article","created":{"date-parts":[[2018,3,8]],"date-time":"2018-03-08T01:03:50Z","timestamp":1520471030000},"page":"17-20","source":"Crossref","is-referenced-by-count":4,"title":["Retinitis pigmentosa and deafness"],"prefix":"10.1177","volume":"80","author":[{"given":"R P","family":"Mills","sequence":"first","affiliation":[{"name":"ENT Department, King's College Hospital, London SE5"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"D M","family":"Calver","sequence":"additional","affiliation":[{"name":"Eye Department, Guy's Hospital, London SE1"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"179","published-online":{"date-parts":[[1987,1,1]]},"reference":[{"key":"bibr1-014107688708000108","first-page":"250","volume":"4","author":"Von Graeffe 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