Literature DB >> 11179024

A progressive autosomal recessive cataract locus maps to chromosome 9q13-q22.

E Héon1, A D Paterson, M Fraser, G Billingsley, M Priston, A Balmer, D F Schorderet, A Verner, T J Hudson, F L Munier.   

Abstract

Cataracts are the leading cause of blindness in most countries. Although most hereditary cases appear to follow an autosomal dominant pattern of inheritance, autosomal recessive inheritance has been clearly documented and is probably underrecognized. We studied a large family-from a relatively isolated geographic region-whose members were affected by autosomal recessive adult-onset pulverulent cataracts. We mapped the disease locus to a 14-cM interval at a novel disease locus, 9q13-q22 (between markers D9S1123 and D9S257), with a LOD score of 4.7. The study of this progressive and age-related cataract phenotype may provide insight into the cause of the more common sporadic form of age-related cataracts.

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Year:  2001        PMID: 11179024      PMCID: PMC1274489          DOI: 10.1086/318798

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  28 in total

1.  Are intraocular lenses the solution to cataract blindness in Africa?

Authors:  D Yorston
Journal:  Br J Ophthalmol       Date:  1998-05       Impact factor: 4.638

2.  The genetics of cataract: our vision becomes clearer.

Authors:  J F Hejtmancik
Journal:  Am J Hum Genet       Date:  1998-03       Impact factor: 11.025

3.  Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA.

Authors:  M Litt; P Kramer; D M LaMorticella; W Murphey; E W Lovrien; R G Weleber
Journal:  Hum Mol Genet       Date:  1998-03       Impact factor: 6.150

4.  Mapping of new recessive cataract gene (lr2) in the mouse.

Authors:  C W Song; M Okumoto; N Mori; J S Kim; S S Han; K Esaki
Journal:  Mamm Genome       Date:  1997-12       Impact factor: 2.957

5.  Hereditary hyperferritinemia-cataract syndrome: two novel mutations in the L-ferritin iron-responsive element.

Authors:  A D Mumford; T Vulliamy; J Lindsay; A Watson
Journal:  Blood       Date:  1998-01-01       Impact factor: 22.113

6.  A missense mutation in the human connexin50 gene (GJA8) underlies autosomal dominant "zonular pulverulent" cataract, on chromosome 1q.

Authors:  A Shiels; D Mackay; A Ionides; V Berry; A Moore; S Bhattacharya
Journal:  Am J Hum Genet       Date:  1998-03       Impact factor: 11.025

7.  The gamma-crystallins and human cataracts: a puzzle made clearer.

Authors:  E Héon; M Priston; D F Schorderet; G D Billingsley; P O Girard; N Lubsen; F L Munier
Journal:  Am J Hum Genet       Date:  1999-11       Impact factor: 11.025

8.  Vision for the world.

Authors:  A S Lim
Journal:  Eur J Ophthalmol       Date:  1996 Jan-Mar       Impact factor: 1.922

9.  Comprehensive human genetic maps: individual and sex-specific variation in recombination.

Authors:  K W Broman; J C Murray; V C Sheffield; R L White; J L Weber
Journal:  Am J Hum Genet       Date:  1998-09       Impact factor: 11.025

10.  Chromosomal localization of a new mouse lens opacity gene (lop18)

Authors:  B Chang; N L Hawes; R S Smith; J R Heckenlively; M T Davisson; T H Roderick
Journal:  Genomics       Date:  1996-08-15       Impact factor: 5.736

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  29 in total

1.  Molecular genetic analysis of autosomal dominant late-onset cataract in a Chinese Family.

Authors:  Guohua Yang; Shan Zhong; Xianrong Zhang; Biwen Peng; Jun Li; Tie Ke; Hua Xu
Journal:  J Huazhong Univ Sci Technolog Med Sci       Date:  2010-12-22

2.  Autosomal recessive juvenile onset cataract associated with mutation in BFSP1.

Authors:  Ramya Devi Ramachandran; Vijayalakshmi Perumalsamy; J Fielding Hejtmancik
Journal:  Hum Genet       Date:  2007-01-16       Impact factor: 4.132

Review 3.  Inherited Congenital Cataract: A Guide to Suspect the Genetic Etiology in the Cataract Genesis.

Authors:  Olga Messina-Baas; Sergio A Cuevas-Covarrubias
Journal:  Mol Syndromol       Date:  2017-02-07

4.  A missense mutation in the LIM2 gene is associated with autosomal recessive presenile cataract in an inbred Iraqi Jewish family.

Authors:  Eran Pras; Etgar Levy-Nissenbaum; Tangiz Bakhan; Hadas Lahat; Ehud Assia; Noa Geffen-Carmi; Moshe Frydman; Boleslaw Goldman; Elon Pras
Journal:  Am J Hum Genet       Date:  2002-03-26       Impact factor: 11.025

5.  Locus heterogeneity in autosomal recessive congenital cataracts: linkage to 9q and germline HSF4 mutations.

Authors:  Tim Forshew; Colin A Johnson; Shagufta Khaliq; Shanaz Pasha; Catherine Willis; Rashida Abbasi; Louise Tee; Ursula Smith; Richard C Trembath; Syed Qasim Mehdi; Anthony T Moore; Eamonn R Maher
Journal:  Hum Genet       Date:  2005-06-16       Impact factor: 4.132

6.  Coexistence of mal de Meleda and congenital cataract in a consanguineous Tunisian family: two case reports.

Authors:  Mbarka Bchetnia; Ahlem Merdassi; Cherine Charfeddine; Fatma Mgaieth; Selma Kassar; Farah Ouechtati; Ibtissem Chouchene; Hamouda Boussen; Mourad Mokni; Amel Dhahri-Ben Osman; Med Samir Boubaker; Sonia Abdelhak; Leila Elmatri
Journal:  J Med Case Rep       Date:  2010-04-20

7.  Autosomal recessive congenital cataract linked to EPHA2 in a consanguineous Pakistani family.

Authors:  Haiba Kaul; S Amer Riazuddin; Mariam Shahid; Samra Kousar; Nadeem H Butt; Ahmad U Zafar; Shaheen N Khan; Tayyab Husnain; Javed Akram; J Fielding Hejtmancik; Sheikh Riazuddin
Journal:  Mol Vis       Date:  2010-03-24       Impact factor: 2.367

8.  Autosomal recessive congenital cataract in consanguineous Pakistani families is associated with mutations in GALK1.

Authors:  Afshan Yasmeen; S Amer Riazuddin; Haiba Kaul; Sadia Mohsin; Mohsin Khan; Zaheeruddin A Qazi; Idrees A Nasir; Ahmad U Zafar; Shaheen N Khan; Tayyab Husnain; Javed Akram; J Fielding Hejtmancik; Sheikh Riazuddin
Journal:  Mol Vis       Date:  2010-04-15       Impact factor: 2.367

Review 9.  Cat-Map: putting cataract on the map.

Authors:  Alan Shiels; Thomas M Bennett; J Fielding Hejtmancik
Journal:  Mol Vis       Date:  2010-10-08       Impact factor: 2.367

10.  A new locus for autosomal recessive congenital cataract identified in a Pakistani family.

Authors:  Haiba Kaul; S Amer Riazuddin; Afshan Yasmeen; Sadia Mohsin; Mohsin Khan; Idrees A Nasir; Shaheen N Khan; Tayyab Husnain; Javed Akram; J Fielding Hejtmancik; Sheikh Riazuddin
Journal:  Mol Vis       Date:  2010-02-16       Impact factor: 2.367

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