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      [The Hallermann-Streiff syndrome in 2 generations].

      , ,
      Ceskoslovenska oftalmologie

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          Abstract

          The authors discuss a rare case, unique in our literature, of the familial incidence of Hallermann-Streiff's syndrome and the treatment of some of its complications. Special emphasis is laid on genetic analysis which provides evidence of autosomal dominant heredity with a variable expressivity of the pathological gene, and which must be applied in genetic consultations.

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          Author and article information

          Journal
          Cesk Oftalmol
          Ceskoslovenska oftalmologie
          0009-059X
          0009-059X
          Sep 1989
          : 45
          : 5
          Article
          2805105
          1b720cec-f38d-4c4c-ba15-1c660c1f773d
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