Literature DB >> 8004098

Localization of the gene for dominant cystoid macular dystrophy on chromosome 7p.

H Kremer1, A Pinckers, B van den Helm, A F Deutman, H H Ropers, E C Mariman.   

Abstract

In a family with autosomal dominant cystoid macular dystrophy (DCMD) linkage was detected with the dinucleotide marker D7S435 on the short arm of chromosome 7. With markers flanking D7S435, the DCMD locus could be assigned to the interval D7S493-D7S526 at 7p15-p21, which spans approximately 20 cM. Three-point linkage yielded a maximal lod score of 9.46 and location score of 43.5 and suggested that DCMD is 5,5 cM proximal to D7S493. Recently, a retinitis pigmentosa (RP7) locus has been mapped in roughly the same area of chromosome 7. Genetic data of both studies described below, allow a region of overlap between the location of the DCMD and the RP7 gene between D7S435 and D7S526. Both genes being one and the same will further substantiate the close relationship between macular degeneration and retinitis pigmentosa.

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Year:  1994        PMID: 8004098     DOI: 10.1093/hmg/3.2.299

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  17 in total

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Authors:  H van Bokhoven; M Jung; A P Smits; S van Beersum; F Rüschendorf; M van Steensel; M Veenstra; J H Tuerlings; E C Mariman; H G Brunner; T F Wienker; A Reis; H H Ropers; B C Hamel
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Review 2.  Molecular genetics of macular dystrophies.

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3.  The human H-twist gene is located at 7p21 and encodes a B-HLH protein that is 96% similar to its murine M-twist counterpart.

Authors:  P Bourgeois; C Stoetzel; A L Bolcato-Bellemin; M G Mattei; F Perrin-Schmitt
Journal:  Mamm Genome       Date:  1996-12       Impact factor: 2.957

4.  Exclusion of atypical vitelliform macular dystrophy from 8q24.3 and from other known macular degenerative loci.

Authors:  M M Sohocki; L S Sullivan; H A Mintz-Hittner; K Small; R E Ferrell; S P Daiger
Journal:  Am J Hum Genet       Date:  1997-07       Impact factor: 11.025

Review 5.  Genotype-phenotype correlations and differential diagnosis in autosomal dominant macular disease.

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7.  Dominant cystoid macular dystrophy associated with mutations in the RP1L1 gene.

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Review 8.  Recent advances in the gene map of inherited eye disorders: primary hereditary diseases of the retina, choroid, and vitreous.

Authors:  P J Rosenfeld; V A McKusick; J S Amberger; T P Dryja
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9.  Mutations in the human TBX4 gene cause small patella syndrome.

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Journal:  Am J Hum Genet       Date:  2004-04-21       Impact factor: 11.025

Review 10.  The genetics of inherited macular dystrophies.

Authors:  M Michaelides; D M Hunt; A T Moore
Journal:  J Med Genet       Date:  2003-09       Impact factor: 6.318

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