Literature DB >> 2805105

[The Hallermann-Streiff syndrome in 2 generations].

A Gerinec, B Spissáková, M Chynoranský.   

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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Year:  1989        PMID: 2805105

Source DB:  PubMed          Journal:  Cesk Oftalmol        ISSN: 0009-059X


  3 in total

1.  Hallermann-Streiff syndrome diagnosed in the seventh decade of life.

Authors:  Ayaka Shimada; Yuji Takayanagi; Sho Ichioka; Akiko Ishida; Masaki Tanito
Journal:  Am J Ophthalmol Case Rep       Date:  2022-05-25

2.  Hallermann-Streiff Syndrome: No Evidence for a Link to Laminopathies.

Authors:  F Kortüm; M Chyrek; S Fuchs; B Albrecht; G Gillessen-Kaesbach; U Mütze; E Seemanova; S Tinschert; D Wieczorek; G Rosenberger; K Kutsche
Journal:  Mol Syndromol       Date:  2011-11-12

3.  Hallermann-Streiff syndrome with uncommon ocular features, ultrasound biomicroscopy and optical coherence tomography findings: A case report.

Authors:  Wei Shen; Min Dai; Yunshan Su; Qing Zhang; Hongsong Li
Journal:  Medicine (Baltimore)       Date:  2019-12       Impact factor: 1.889

  3 in total

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