Literature DB >> 9135408

Usher syndrome in the city of Birmingham--prevalence and clinical classification.

C I Hope1, S Bundey, D Proops, A R Fielder.   

Abstract

AIMS: To estimate the prevalence of Usher syndrome in the city of Birmingham, and to establish a database of patients who have been classified into different clinical subtypes essential for future gene mutation analysis.
METHODS: Symptomatic cases of Usher syndrome (US) resident in the city of Birmingham in June 1994 were ascertained through multiple sources. Ophthalmic and audiological reassessment together with examination of medical records and patient questionnaires allowed classification of three subtypes, US 1, US 2, and US 3. In addition, family pedigrees were examined and blood was taken from index patients for DNA extraction.
RESULTS: In the population aged over 15 years the prevalence was 6.2 per 100 000 population for all US subtypes. The prevalence for US 1 and US 2 was 5.3 per 100 000 population. This is greater than previously reported. In the age group 30-49 years the prevalence approached 1 in 10 000. Clinical classification found 33% US 1, 47% US 2, and 20% US 3.
CONCLUSION: This higher prevalence rate and greater frequency of US 2 and US 3 may reflect a more complete ascertainment.

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Year:  1997        PMID: 9135408      PMCID: PMC1721995          DOI: 10.1136/bjo.81.1.46

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN: 0007-1161            Impact factor:   4.638


  28 in total

1.  Usher syndrome: an otoneurologic study.

Authors:  C G Möller; W J Kimberling; S L Davenport; I Priluck; V White; K Biscone-Halterman; L M Odkvist; P E Brookhouser; G Lund; T J Grissom
Journal:  Laryngoscope       Date:  1989-01       Impact factor: 3.325

2.  Usher syndrome: clinical findings and gene localization studies.

Authors:  W J Kimberling; C G Möller; S L Davenport; G Lund; T J Grissom; I Priluck; V White; M D Weston; K Biscone-Halterman; P E Brookhouser
Journal:  Laryngoscope       Date:  1989-01       Impact factor: 3.325

3.  Localization of Usher syndrome type II to chromosome 1q.

Authors:  W J Kimberling; M D Weston; C Möller; S L Davenport; Y Y Shugart; I A Priluck; A Martini; M Milani; R J Smith
Journal:  Genomics       Date:  1990-06       Impact factor: 5.736

4.  Estimation of prognosis and prevalence of retinitis pigmentosa and Usher syndrome in Norway.

Authors:  J Grøndahl
Journal:  Clin Genet       Date:  1987-04       Impact factor: 4.438

5.  Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11.

Authors:  W J Kimberling; C G Möller; S Davenport; I A Priluck; P H Beighton; J Greenberg; W Reardon; M D Weston; J B Kenyon; J A Grunkemeyer
Journal:  Genomics       Date:  1992-12       Impact factor: 5.736

6.  A gene for Usher syndrome type I (USH1A) maps to chromosome 14q.

Authors:  J Kaplan; S Gerber; D Bonneau; J M Rozet; O Delrieu; M L Briard; H Dollfus; I Ghazi; J L Dufier; J Frézal
Journal:  Genomics       Date:  1992-12       Impact factor: 5.736

7.  Usher syndrome: results of a screening program in Colombia.

Authors:  M L Tamayo; J E Bernal; G E Tamayo; J L Frias; G Alvira; O Vergara; V Rodriguez; J I Uribe; J C Silva
Journal:  Clin Genet       Date:  1991-10       Impact factor: 4.438

8.  Mapping recessive ophthalmic diseases: linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1q.

Authors:  R A Lewis; B Otterud; D Stauffer; J M Lalouel; M Leppert
Journal:  Genomics       Date:  1990-06       Impact factor: 5.736

9.  Usher syndrome in four Norwegian counties.

Authors:  J Grøndahl; S Mjøen
Journal:  Clin Genet       Date:  1986-07       Impact factor: 4.438

10.  Causes of childhood deafness at a Dutch school for the hearing impaired.

Authors:  P M van Rijn; C W Cremers
Journal:  Ann Otol Rhinol Laryngol       Date:  1991-11       Impact factor: 1.547

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  46 in total

Review 1.  Genetics and pathological mechanisms of Usher syndrome.

Authors:  Denise Yan; Xue Z Liu
Journal:  J Hum Genet       Date:  2010-04-09       Impact factor: 3.172

2.  Novel mutations in the long isoform of the USH2A gene in patients with Usher syndrome type II or non-syndromic retinitis pigmentosa.

Authors:  Terri L McGee; Babak Jian Seyedahmadi; Meredith O Sweeney; Thaddeus P Dryja; Eliot L Berson
Journal:  J Med Genet       Date:  2010-05-27       Impact factor: 6.318

3.  MYO7A mutation screening in Usher syndrome type I patients from diverse origins.

Authors:  T Jaijo; E Aller; M Beneyto; C Najera; C Graziano; D Turchetti; M Seri; C Ayuso; M Baiget; F Moreno; C Morera; H Perez-Garrigues; J M Millan
Journal:  J Med Genet       Date:  2007-03       Impact factor: 6.318

4.  A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss.

Authors:  Inga Ebermann; Hendrik P N Scholl; Peter Charbel Issa; Elvir Becirovic; Jürgen Lamprecht; Bernhard Jurklies; José M Millán; Elena Aller; Diana Mitter; Hanno Bolz
Journal:  Hum Genet       Date:  2006-12-15       Impact factor: 4.132

5.  Children with Usher syndrome: mental and behavioral disorders.

Authors:  Jesper Dammeyer
Journal:  Behav Brain Funct       Date:  2012-03-27       Impact factor: 3.759

6.  CEP78 is mutated in a distinct type of Usher syndrome.

Authors:  Qing Fu; Mingchu Xu; Xue Chen; Xunlun Sheng; Zhisheng Yuan; Yani Liu; Huajin Li; Zixi Sun; Huiping Li; Lizhu Yang; Keqing Wang; Fangxia Zhang; Yumei Li; Chen Zhao; Ruifang Sui; Rui Chen
Journal:  J Med Genet       Date:  2016-09-14       Impact factor: 6.318

7.  Coats-like lesions in Usher syndrome type II.

Authors:  Hayyam Kiratli; Cem Oztürkmen
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2003-12-03       Impact factor: 3.117

8.  Survey in to the prevalence of hearing loss in patients diagnosed with retinitis pigmentosa.

Authors:  Satoshi Iwasaki; Yuuka Maruyama; Yoshihiro Hotta; Yasuyuki Hashimoto; Mitsuyoshi Nagura
Journal:  Int Ophthalmol       Date:  2006-03-07       Impact factor: 2.031

9.  Mutation analysis in the long isoform of USH2A in American patients with Usher Syndrome type II.

Authors:  Denise Yan; Xiaomei Ouyang; D Michael Patterson; Li Lin Du; Samuel G Jacobson; Xue-Zhong Liu
Journal:  J Hum Genet       Date:  2009-10-30       Impact factor: 3.172

10.  Genetic analysis through OtoSeq of Pakistani families segregating prelingual hearing loss.

Authors:  Mohsin Shahzad; Theru A Sivakumaran; Tanveer A Qaiser; Julie M Schultz; Zawar Hussain; Megan Flanagan; Munir A Bhinder; Diane Kissell; John H Greinwald; Shaheen N Khan; Thomas B Friedman; Kejian Zhang; Saima Riazuddin; Sheikh Riazuddin; Zubair M Ahmed
Journal:  Otolaryngol Head Neck Surg       Date:  2013-06-14       Impact factor: 3.497

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