Literature DB >> 11527934

Locus for autosomal recessive nonsyndromic persistent hyperplastic primary vitreous.

S Khaliq1, A Hameed, M Ismail, K Anwar, B Leroy, A M Payne, S S Bhattacharya, S Q Mehdi.   

Abstract

PURPOSE: To map the disease locus in a six-generation, consanguineous Pakistani family affected by nonsyndromic autosomal recessive persistent hyperplastic primary vitreous (arPHPV). All affected individuals had peripheral anterior synechiae and corneal opacities with variable degrees of cataract and a retrolenticular white mass behind the lens.
METHODS: Genomic DNA from family members was typed for alleles at more than 400 known polymorphic genetic markers, by polymerase chain reaction. Alleles were assigned to individuals, which allowed calculation of lod scores.
RESULTS: A maximum two-point lod score of 4.07 was obtained with marker D10S1225 with no recombination. Two recombinations with marker D10S208 and D10S537 localized the disease within a region of approximately 30 centimorgans (cM). However, homozygosity across the region refined the arPHPV locus to 13 cM.
CONCLUSIONS: Linkage analysis shows localization of nonsyndromic arPHPV to chromosome10q11-q21.

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Year:  2001        PMID: 11527934

Source DB:  PubMed          Journal:  Invest Ophthalmol Vis Sci        ISSN: 0146-0404            Impact factor:   4.799


  11 in total

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4.  Surgical treatment and visual outcomes of cataract with persistent hyperplastic primary vitreous.

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7.  Microphthalmia, persistent hyperplastic hyaloid vasculature and lens anomalies following overexpression of VEGF-A188 from the alphaA-crystallin promoter.

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8.  Clinical characteristics and treatment of 22 eyes of morning glory syndrome associated with persistent hyperplastic primary vitreous.

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Review 10.  Complex genetics of familial exudative vitreoretinopathy and related pediatric retinal detachments.

Authors:  Hiroyuki Kondo
Journal:  Taiwan J Ophthalmol       Date:  2015-06-06
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