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Syndromes of genetic juvenile retinal detachment

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Abstract

Childhood retinal detachment while not common is usually severe, more often accompanied by severe myopia and more often hereditary and syndromal in nature than is retinal detachment which occurs in the middle aged to elderly individual. — 6 of these syndromes, are presented and their clinical features described.

Zusammenfassung

Die Netzhautablösung im Kindesalter kommt zwar selten vor, ist aber gewöhnlich schwer und oft begleitet von schwerer Kurzsichtigkeit und ebenfalls häufig erblich oder syndromgebunden. Sie steht damit im Gegensatz zur Netzhautablösung bei älteren Patienten. — 6 dieser Syndrome und ihre klinische Symptomatik werden hier vorgestellt.

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Authors and Affiliations

  1. Division of Oral Pathology, School of Dentistry, University of Minnesota, Minneapolis, USA

    Robert J. Gorlin & William H. Knobloch

  2. Department of Ophthalmology, University of Minnesota Hospitals, Minneapolis, USA

    Robert J. Gorlin & William H. Knobloch

Authors
  1. Robert J. Gorlin
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  2. William H. Knobloch
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Additional information

This paper was made possible in part by U.S.P.H.S. Program Grant in Oral Pathology DE-1770.

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Gorlin, R.J., Knobloch, W.H. Syndromes of genetic juvenile retinal detachment. Z. Kinder-Heilk. 113, 81–92 (1972). https://doi.org/10.1007/BF00473403

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  • DOI: https://doi.org/10.1007/BF00473403

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