Clinical and genetic evidence for autosomal dominant North Carolina macular dystrophy in a German family.
作者信息
Pauleikhoff D, Sauer C G, Müller C R, Radermacher M, Merz A, Weber B H
机构信息
Department of Ophthalmology, St Franziskus-Hospital, Würzburg, Germany.
出版信息
Am J Ophthalmol. 1997 Sep;124(3):412-5. doi: 10.1016/s0002-9394(14)70842-6.
PURPOSE
To describe a German family with clinical and genetic evidence of autosomal dominant North Carolina macular dystrophy.
METHODS
Twenty-six individuals from a five-generation family from northern Germany were investigated clinically. In addition, we performed genetic linkage analyses using polymorphic markers from proximal 6q.
RESULTS
The affected family members showed clinical abnormalities consistent with North Carolina macular dystrophy including multiple drusen, choroidal neovascularization in one patient, and geographic atrophy in elderly patients. The DNA analyses demonstrated significant linkage to the North Carolina macular dystrophy locus on chromosome 6q14-q16.2.
CONCLUSION
Our findings provide strong evidence of a German pedigree with an autosomal dominant macular dystrophy manifesting with clinical abnormalities consistent with North Carolina macular dystrophy.
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