Usher syndrome type III (USH3): The clinical manifestations in 42 patients

References

• Abraham F A., Cohen D, Sohmer H. Usher's Syndrome: Electrophysiological tests of the visual and auditory systems. Doc Ophthalmol 44 1977; 2: 435–444
   Google Scholar
• Beatty C W., McDonald T J., Colvard D M. Usher's syndrome with unusual otologic manifestation. Mayo clinic proc 1979; 54: 543–546
   Google Scholar
• Belal A. Usher's Syndrome. A temporal bone report. J Laryngol Otol 1975; 89: 175–181
   Google Scholar
• Davenport S LH, Omenn G S. (1977) The heterogeneity of Usher syndrome. Fifth International Conference on Birth Defects, Montreal, Canada, 1977, 87–88, 21–27.8 Abstracts of Papers
   Google Scholar
• Fishman G A., Kumar A J., Maurice E, Torok N, Anderson R J. Usher's Syndrome, Ophthalmic and Neuro-otologic Findings Suggesting Genetic Heterogeneity. Arch Ophthalmol 1983; 101: 1367–1374
   PubMedGoogle Scholar
• Gorlin R J., Tilsner T J., Feinstein S, Duvall A J. Usher's Syndrome Type 3. Arch Otolaryngol 1979; 105: 353–354
   PubMedGoogle Scholar
• Hallgren B. Retinitis pigmentosa combined with congenital deafness; with vestibulocerebellar ataxia and mental abnormality in a proportion of cases. A clinical and genetico-statistical study. Acta Psychiatry et Neurol Scand 1959; 34(suppl 138)5–101
   Google Scholar
• Kaitalo H. Kuurosokeat Suomessa, osa1: Vamman määrittely ja tunnistaminen, Kuopion yliopiston julkaisuja, H. Kaitalo. Publications of Kuopio University. 1990, The Deaf-Blinds in Finland. Part I: The Definition and recognition of the Handicap, in Finnish)
   Google Scholar
• Kaplan J, Gerber S, Bonneau D, Rozet J M., Delrieu O, Briard M L., Dollfus H, Ghazi I, Dufier J L., Frezal J, Munnich A. A gene for Usher Syndrome Type 1 (USH1A) maps to chromosome 14q. Genomics 1992; 14: 979–987
   PubMed Web of Science ®Google Scholar
• Karjalainen S, Pakarinen L, Kääriäinen H, Teräsvirta M, Vartiainen E. Progressive hearing loss in Usher's Syndrome. Ann Otol Rhinol Laryngol 11 1989; 198: 863–866
   Google Scholar
• Karjalainen S, Teräsvirta M, Kärjä J, Kääriäinen H. An unusual otological manifestation of Usher's Syndrome in four siblings. Clin Gen 1983; 4: 273–279
   Google Scholar
• Karjalainen S, Teräsvirta M, Kärjä J, Kääriäinen H. Usher's Syndrome Type 3: ENG findings in four affected and six unaffected siblings. J Laryngol Otol 1985; 99: 43–48
   PubMed Web of Science ®Google Scholar
• Karp A, Santore A. Retinitis pigmentosa and progressive hearing loss. J Speech Hear Dis 1983; 48: 308–314
   PubMedGoogle Scholar
• Kimberling W J., Möller C G., Davenport S LH, Lund G, Grissom T J., Priluck I, White V, Weston M D., Biscone-Halterman K, Brookhouser P E. Usher Syndrome: Clinical Findings and Gene Localization Studies. Laryngoscope 1989; 99: 66–72
   PubMed Web of Science ®Google Scholar
• Kimberling W J., Möller C G., Davenport S, Priluck I A., Beighton P H., Greenberg J, Reardon W, Weston M D., Kenyon J B., Grunkemeyer J A., Pieke Dahl S, Overbeck L D., Blackwood D J., Brower A M., Hoover D M., Rowland P, Smith J H. Linkage of Usher Syndrome Type 1 gene (USH1B) to the long arm of chromosome 11. Genomics 1992; 14: 988–994
   PubMed Web of Science ®Google Scholar
• Kimberling W J., Weston M D., Möller C, Davenport S LH, Shugart Y Y., Priluck I A., Martini A, Milani M, Smith R. Localization of Usher Syndrome Type II to chromosome 1q. Genomics 1990; 7: 245–249
   PubMed Web of Science ®Google Scholar
• Kimberling W J., Weston D W., Möller C, van Aarem A, Cremers C WR, Sumegi J, Ing P S., Connoly C, Martini A, Milani M, Tamayo M L., Bernal J, Greenberg J, Ayuso C. Gene mapping of Usher Syndrome Type IIa: Localization of the Gene to a 2.1 cM Segment on Chromosome 1q41. Am J Hum Genet 1995; 56: 216–223
   PubMedGoogle Scholar
• Kumar A, Fishman G, Torok N. Vestibular and auditory function in Usher's Syndrome. Ann Otol Rhinol Laryngol 1984; 93: 600–608
   PubMed Web of Science ®Google Scholar
• Lewis R A., Otterud B, Stauffer D, Lalouel J M., Leppert M. Mapping recessive ophthalmic disease: Linkage of the locus for Usher Syndrome Type II to a DNA marker on chromosome 1q. Genomics 1990; 7: 250–256
   PubMedGoogle Scholar
• Marmor M F. The electroretinogram in Retinitis Pigmentosa. Arch Ophthalmol 1979; 97: 1300–1304
   Google Scholar
• McLeod A, McConnel F F., Sweeney A, Cooper M C., Nance W E. Clinical variations in Usher's Syndrome. Arch Otolaryngol 1971; 94: 321–334
   Google Scholar
• Merin S, Abraham F A., Auerbach E. Usher's and Hallgren's Syndrome. Acta Gen. Med. Gemello (Roma) 1973; 23: 49–55
   Google Scholar
• Möller C G., Kimberling W J., Davenport S LH, Priluck I, White V, Biscone-Halterman K, Ödkvist L M., Brookhouser P E., Lund G, Grissom T J. Usher Syndrome: An otoneurologic study. Laryngoscope 1989; 99: 73–79
   PubMed Web of Science ®Google Scholar
• Nuutila A. Dystrofia retinitis pigmentosa-dysacusis syndrome (DRD): A study of the Usher or Hallgren Syndrome. J Gen Hum 18 1970; 1: 57–88
   Google Scholar
• Pakarinen L, Karjalainen S, Simola K OJ, Laippala P, Kaitalo H. Usher's Syndrome Type 3 in Finland. Laryngoscope 1995; 105: 613–617
   PubMed Web of Science ®Google Scholar
• Pieke Dahl S, Kimberling W J., Gorin M B., Furman J MR, Pikus A, Möller C. Genetic heterogeneity of Usher Syndrome Type II. J Med Genet 1993; 30: 843–848
   PubMedGoogle Scholar
• Sankila E M., Pakarinen L, de la Chapelle A, Kääriäinen H, Karjalainen S. Assignment of an Usher Syndrome Type III (USH3) Gene to Chromosome 3q. Hum Mol Gen 1995; 4/1: 93–98
   Google Scholar
• Sharp C W., Muir W J., Blackwood D HR, Walker M, Gorden C, St Clair D. M. Schizophrenia and Mental Retardation Associated in a Pedigree With Retinitis Pigmentosa and Sensorineural deafness. Am J Med Gen 1994; 54: 354–360
   Google Scholar
• Smith R JH, Berlin C I., Hejtmancik J F., Keats B JB, Kimberling W J., Lewis R A., Möller C G., Pelias M Z., Tranebjaerg L. Clinical Diagnosis of the Usher Syndromes. Am J Med Gen 1994; 50: 32–38
   PubMed Web of Science ®Google Scholar
• Usher C H. On the inheritance of retinitis pigmentosa with notes of cases. R Lond Ophthalmol Hosp Rep 1914; 19: 130–236
   Google Scholar
• Vernon M. Usher's Syndrome-deafness and progressive blindness: Clinical case, prevention, theory and literature survey. J Chronic Diseases 1969; 22: 133–151
   PubMedGoogle Scholar
• Weil D, Blanchard S, Kaplan J, Guilford P, Gibson F, Walsh J, Mburu P, Varela A, Levilliers J, Weston M D., Kelley P M., Kimberling W J., Wagenaar M, Levi-Acobas F, Larget-Piet D, Munnich A, Steel K P., Brown S D., Petit C. Defective myosin VII gene responsible for Usher Syndrome Type 1B. Nature 1995; 374: 60–61
   PubMed Web of Science ®Google Scholar