期刊文献+

染色体12q15-q23中间缺失和周边角膜异常患者的临床和分子特征

Clinical and molecular characterization of a patient with an interstitial deletion of chromosome 12q15-q23 and peripheral corneal abnormalities
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摘要 PURPOSE: To describe the ocular features of a patient with an interstitial deletion of chromosome 12 and to determine the molecular boundaries of the deletion. DESIGN: Observational case report and laboratory investigation. METHODS: A patient with an interstitial deletion of chromosome 12 was clinically examined for ocular abnormalities. DNA samples were used for molecular studies to define the deletion boundaries. RESULTS: Ocular examination showed abnormalities of the anterior segment consistent with a diagnosis of cornea plana. Molecular analyses showed the deletion included the KERA gene,the SLRP (small leucine repeat protein) gene cluster,the genetic loci for autosomal-dominant (CNA1) and autosomalrecessive (CNA2) cornea plana,and a portion of the mapped locus for high myopia (MYP3). CONCLUSIONS: These results,combined with previous genetic linkage studies,identifies a 3-cM region located between microsatellite markers D12S82 and D12S351 that is likely to contain a gene responsible for CNA1. PURPOSE: To describe the ocular features of a patient with an interstitial deletion of chromosome 12 and to determine the molecular boundaries of the deletion. DESIGN: Observational case report and laboratory investigation. METHODS: A patient with an interstitial deletion of chromosome 12 was clinically examined for ocular abnormalities. DNA samples were used for molecular studies to define the deletion boundaries. RESULTS: Ocular examination showed abnormalities of the anterior segment consistent with a diagnosis of cornea plana. Molecular analyses showed the deletion included the KERA gene, the SLRP (small leucine repeat protein) gene cluster, the genetic loci for autosomal-dominant (CNA1) and autosomalrecessive (CNA2) cornea plana, and a portion of the mapped locus for high myopia (MYP3) . CONCLUSIONS: These results, combined with previous genetic linkage studies, identifies a 3-cM region located between microsatellite markers D12S82 and D12S351 that is likely to contain a gene responsible for CNA1.
出处 《世界核心医学期刊文摘(眼科学分册)》 2006年第6期12-12,共1页 Digest of the World Core Medical Journals:Ophthalmology
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