Literature DB >> 18066515

[A new locus for an autosomal dominant, non-syndromic hearing impairment (DFNA57) located on chromosome 19p13.2 and overlapping with DFNB15].

D Bönsch1, C M Schmidt, P Scheer, J Bohlender, C Neumann, A am Zehnhoff-Dinnesen, T Deufel.   

Abstract

BACKGROUND: Non-syndromic hearing loss is the most genetically heterogeneous trait known in humans. To date, 54 loci for autosomal dominant non-syndromic sensorineural hearing loss (NSSHL) have been identified by linkage analysis.
METHODS: In this study a German pedigree has been identified segregating a progressive bilateral loss of lower and middle frequencies.
RESULTS: A genome-wide screening and linkage analysis revealed the existence of a new NSSHL locus (DFNA57). The phenotype was mapped to a 10 degrees Mbp interval on chromosome 19p13.2 from 7.8 to 18.2 degrees Mbp, a maximum 2-point LOD score of 3.08 was obtained for the marker D19S586. The region overlaps with the recessive locus DFNB15.
CONCLUSION: The results underline the heterogeneity of hereditary hearing disorders. Identification of genes can help to reach a better understanding of the molecular mechanism of hearing.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18066515     DOI: 10.1007/s00106-007-1633-6

Source DB:  PubMed          Journal:  HNO        ISSN: 0017-6192            Impact factor:   1.284


  18 in total

1.  The HUGO Gene Nomenclature Committee (HGNC).

Authors:  S Povey; R Lovering; E Bruford; M Wright; M Lush; H Wain
Journal:  Hum Genet       Date:  2001-10-24       Impact factor: 4.132

2.  PROMM and deafness: exclusion of ZNF9 as the disease gene in DFNA18 suggests a polygenic origin of the PROMM/DM2 phenotype.

Authors:  D Bönsch; C Neumann; R Lang-Roth; O Witte; A Lamprecht-Dinnesen; T Deufel
Journal:  Clin Genet       Date:  2003-01       Impact factor: 4.438

Review 3.  Genetic epidemiology of hearing impairment.

Authors:  N E Morton
Journal:  Ann N Y Acad Sci       Date:  1991       Impact factor: 5.691

4.  Parametric and nonparametric linkage analysis: a unified multipoint approach.

Authors:  L Kruglyak; M J Daly; M P Reeve-Daly; E S Lander
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

5.  A novel locus for X-linked recessive CMT with deafness and optic neuropathy maps to Xq21.32-q24.

Authors:  H-J Kim; S H Hong; C-S Ki; B-J Kim; J-S Shim; S-H Cho; J-H Park; J-W Kim
Journal:  Neurology       Date:  2005-06-14       Impact factor: 9.910

Review 6.  [Congenital hearing disorders in children. 1: Acquired hearing disorders].

Authors:  M Gross; U Finckh-Krämer; M Spormann-Lagodzinski
Journal:  HNO       Date:  2000-12       Impact factor: 1.284

Review 7.  [Non-syndromic hereditary hearing impairment].

Authors:  R Birkenhäger; A Aschendorff; J Schipper; R Laszig
Journal:  Laryngorhinootologie       Date:  2007-04       Impact factor: 1.057

8.  MYO1F as a candidate gene for nonsyndromic deafness, DFNB15.

Authors:  A H Chen; D A Stephan; T Hasson; K Fukushima; C M Nelissen; A F Chen; A I Jun; A Ramesh; G Van Camp; R J Smith
Journal:  Arch Otolaryngol Head Neck Surg       Date:  2001-08

9.  Sets of short tandem repeat polymorphisms for efficient linkage screening of the human genome.

Authors:  J Dubovsky; V C Sheffield; G M Duyk; J L Weber
Journal:  Hum Mol Genet       Date:  1995-03       Impact factor: 6.150

10.  Bilateral sudden sensorineural hearing loss caused by Charcot-Marie-Tooth disease.

Authors:  Chariton E Papadakis; Jiannis K Hajiioannou; Dionysios E Kyrmizakis; John G Bizakis
Journal:  J Laryngol Otol       Date:  2003-05       Impact factor: 1.469

View more
  5 in total

1.  [A new gene locus for an autosomal-dominant non-syndromic hearing impairment (DFNA 33) is situated on chromosome 13q34-qter].

Authors:  D Bönsch; C-M Schmidt; P Scheer; J Bohlender; C Neumann; A Am Zehnhoff-Dinnesen; T Deufel
Journal:  HNO       Date:  2009-04       Impact factor: 1.284

2.  A novel chromosome 19p13.12 deletion in a child with multiple congenital anomalies.

Authors:  Daniel R Jensen; Donna M Martin; Stephen Gebarski; Trilochan Sahoo; Ellen K Brundage; A Craig Chinault; Edgar A Otto; Moumita Chaki; Friedhelm Hildebrandt; Sau Wai Cheung; Marci M Lesperance
Journal:  Am J Med Genet A       Date:  2009-03       Impact factor: 2.802

Review 3.  Genetics of Tinnitus: Still in its Infancy.

Authors:  Barbara Vona; Indrajit Nanda; Wafaa Shehata-Dieler; Thomas Haaf
Journal:  Front Neurosci       Date:  2017-05-08       Impact factor: 4.677

4.  The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis.

Authors:  Erna V Ivarsdottir; Hilma Holm; Stefania Benonisdottir; Thorhildur Olafsdottir; Gardar Sveinbjornsson; Gudmar Thorleifsson; Hannes P Eggertsson; Gisli H Halldorsson; Kristjan E Hjorleifsson; Pall Melsted; Arnaldur Gylfason; Gudny A Arnadottir; Asmundur Oddsson; Brynjar O Jensson; Aslaug Jonasdottir; Adalbjorg Jonasdottir; Thorhildur Juliusdottir; Lilja Stefansdottir; Vinicius Tragante; Bjarni V Halldorsson; Hannes Petersen; Gudmundur Thorgeirsson; Unnur Thorsteinsdottir; Patrick Sulem; Ingibjorg Hinriksdottir; Ingileif Jonsdottir; Daniel F Gudbjartsson; Kari Stefansson
Journal:  Commun Biol       Date:  2021-06-09

5.  Identifying components of the hair-cell interactome involved in cochlear amplification.

Authors:  Jing Zheng; Charles T Anderson; Katharine K Miller; MaryAnn Cheatham; Peter Dallos
Journal:  BMC Genomics       Date:  2009-03-25       Impact factor: 3.969

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.