Literature DB >> 1415347

Clinical variability and genetic heterogeneity within the Acadian Usher population.

R J Smith1, M Z Pelias, S P Daiger, B Keats, W Kimberling, J F Hejtmancik.   

Abstract

A number of Usher syndrome (USH) families are found among the French-Acadians living in southwestern Louisiana. These families are descended from a few common ancestors, suggesting that USH may be homogeneous within this ethnic group. However, we report distinct phenotypic variability. Based on differences in psychomotor development and tests of auditory and vestibular function, Acadian individuals with both USH Type 1 and Type 2 can be identified. One additional family, with unusual findings, represents a third clinical phenotype. Linkage data strongly support these clinical observations.

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Year:  1992        PMID: 1415347     DOI: 10.1002/ajmg.1320430612

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  6 in total

1.  Tightly linked flanking microsatellite markers for the Usher syndrome type I locus on the short arm of chromosome 11.

Authors:  B J Keats; N Nouri; M Z Pelias; P L Deininger; M Litt
Journal:  Am J Hum Genet       Date:  1994-04       Impact factor: 11.025

2.  Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse origins.

Authors:  A Adato; D Weil; H Kalinski; Y Pel-Or; H Ayadi; C Petit; M Korostishevsky; B Bonne-Tamir
Journal:  Am J Hum Genet       Date:  1997-10       Impact factor: 11.025

3.  Usher syndrome type III (USH3) linked to chromosome 3q in an Italian family.

Authors:  P Gasparini; A De Fazio; A I Croce; P Stanziale; L Zelante
Journal:  J Med Genet       Date:  1998-08       Impact factor: 6.318

Review 4.  Atypical and ultra-rare Usher syndrome: a review.

Authors:  Rosalie M Nolen; Robert B Hufnagel; Thomas B Friedman; Amy E Turriff; Carmen C Brewer; Christopher K Zalewski; Kelly A King; Talah T Wafa; Andrew J Griffith; Brian P Brooks; Wadih M Zein
Journal:  Ophthalmic Genet       Date:  2020-05-06       Impact factor: 1.803

5.  Polymorphism rs7278468 is associated with Age-related cataract through decreasing transcriptional activity of the CRYAA promoter.

Authors:  Xiaoyin Ma; Xiaodong Jiao; Zhiwei Ma; J Fielding Hejtmancik
Journal:  Sci Rep       Date:  2016-03-17       Impact factor: 4.379

Review 6.  Usher Syndrome: Genetics and Molecular Links of Hearing Loss and Directions for Therapy.

Authors:  Meg Whatley; Abbie Francis; Zi Ying Ng; Xin Ee Khoh; Marcus D Atlas; Rodney J Dilley; Elaine Y M Wong
Journal:  Front Genet       Date:  2020-10-22       Impact factor: 4.599

  6 in total

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