Lorenz, Birgit and Preising, Markus N. (2005) Best's disease. Overview of pathology and its causes. OPHTHALMOLOGE, 102 (2). pp. 111-115. ISSN 0941-293X,
Full text not available from this repository. (Request a copy)Abstract
Best's disease is a hereditary affection with reduced penetrance and juvenile on-set. The fundus may be unremarkable or present various stages up to scarring of the macula. Histopathology of advanced stages discloses deposits of lipofuscin on Bruch's membrane, the innermost layer of which is the basal membrane of the retinal pigment epithelum (RPE). The deposits correlate with lipofuscin and melanofuscin granulae in the RPE. Photoreceptors correlating with the lesions have lost their out segments and the RPE as well as the photoreceptors appear edematous. Loss of photoreceptor function does not necessarily follow progression of fundus appearance. Loss of function usually correlates with a reduced Arden ratio of the electro-oculogram even in the absence of funduscopic changes. Best's disease is caused by mutations in VMD2 (hBEST1). Bestrophin, the gene product of hBEST1, is a regulatory part of a Ca2+ channel or a Ca2+-dependant Cl- channel. In this paper the relevent data on clinical and genetic pathology are summarized and evaluated.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | VITELLIFORM MACULAR DYSTROPHY; FAMILY; GENE; IDENTIFICATION; BESTROPHIN; CHANNELS; PROTEIN; VMD2; |
| Subjects: | 600 Technology > 610 Medical sciences Medicine |
| Divisions: | Medicine > Abteilung für Pädiatrische Ophthalmologie, Strabismologie und Ophthalmogenetik |
| Depositing User: | Dr. Gernot Deinzer |
| Date Deposited: | 31 May 2021 07:01 |
| Last Modified: | 31 May 2021 07:01 |
| URI: | https://pred.uni-regensburg.de/id/eprint/36557 |
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