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常染色体显性先天性眼球震颤与6p12、7p11和15q11无连锁关系:一个德国家族的病例报道
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作者 Hoffmann s. Becker A. +2 位作者 hoerle s. B. Hemmer 张少娟 《世界核心医学期刊文摘(眼科学分册)》 2005年第3期37-37,共1页
Purpose Congenital nystagmus (CN) is an eye movement disorder that usually st arts within the first months of life. Autosomal dominant, autosomal recessive, a nd X chromo somal pedigree patterns are observed. Causativ... Purpose Congenital nystagmus (CN) is an eye movement disorder that usually st arts within the first months of life. Autosomal dominant, autosomal recessive, a nd X chromo somal pedigree patterns are observed. Causative genes are yet unknown. Several loci were implicated to contain disease relevant genes for autosomal dominant CN (AD CN). AD CN cosegregated with a balanced translocation of 7;15 in a family . In a large black pedigree linkage was demonstrated to 6p12. Design In this stu dy, we describe a large German family with AD congenital nystagmus. Linkage of A D in this family was tested with previously implicated loci. Methods Affected fa mily members and unaffected members underwent genetic analysis. Key family membe rs underwent ophthalmologic testing and oculography. Results No linkage of AD CN to the implicated loci on 6p12, and 7p11, and 15q11 was found in this study. Co nclusion In the presented pedigree genes on 15q11, and on the assumption of full penetrance, 6p12 and 7p11 are not involved in the development of AD congenital nystagmus. 展开更多
关键词 先天性眼球震颤 Q11 常染色体 连锁关系 眼科检查 运动障碍性疾病 基因位点 致病基因 基因分析 遗传性疾病
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