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Familiäre juvenile Makuladystrophie mit kongenitaler Hypotrichosis capitis -- Familial juvenile macular dystrophy with congenital hypotrichosis capitis

Becker, M, Rohrschneider, K, Tilgen, W, Weber, Bernhard H. F. and Völcker, H E (1998) Familiäre juvenile Makuladystrophie mit kongenitaler Hypotrichosis capitis -- Familial juvenile macular dystrophy with congenital hypotrichosis capitis. Der Ophthalmologe 95 (4), pp. 233-240.

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Abstract

Background: Our knowledge about the pathogenesis of hereditary macular diseases is still very circumscript. For genetic determination, a knowledge of the coincidence of eye symptoms and other defined common symptoms is helpful. The purpose of this paper was to present two sisters of a family of consanguineous parents with the combination of hypotrichosis of the head and macular dystrophy in the ...

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Item type:Article
Date:1998
Institutions:Medicine > Lehrstuhl für Humangenetik
Identification Number:
ValueType
10.1007/s003470050268DOI
9623260PubMed ID
Keywords:Macular dystrophy; Hypotrichosis capitis; Ectodermal dysplasia; Fundus perimetry
Dewey Decimal Classification:600 Technology > 610 Medical sciences Medicine
Status:Published
Refereed:Yes, this version has been refereed
Created at the University of Regensburg:No
Item ID:35497
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