Literature DB >> 1815166

Congenital alacrima without associated manifestations (AD). An affected father and son.

S M Hegab1, S M Sheriff, E S el-Aasar, E A Lashin, C I Phillips.   

Abstract

The authors report a Kuwaiti Arab family in which the father and one of his two sons have severe hypolacrimation with blotchy staining of the cornea and punctate staining of the interpalpebral bulbar conjunctiva by fluorescein and Rose Bengal. Pharmacologic testing together with biochemical analysis and systemic examinations and investigations suggest an isolated dysfunction of lacrimation. The authors' small Arab family differs from the only other recorded pedigree (Irish) in which all five affected members in four generations also had atopy.

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Year:  1991        PMID: 1815166     DOI: 10.3109/13816819109025811

Source DB:  PubMed          Journal:  Ophthalmic Paediatr Genet        ISSN: 0167-6784


  2 in total

1.  Tear protein analysis in presumed congenital alacrima.

Authors:  Shigeharu Yaginuma; Yoko Akune; Chika Shigeyasu; Yoji Takano; Masakazu Yamada
Journal:  Clin Ophthalmol       Date:  2018-12-11

Review 2.  Hypolacrimia and Alacrimia as Diagnostic Features for Genetic or Congenital Conditions.

Authors:  Marjolaine Willems; Constance F Wells; Christine Coubes; Marie Pequignot; Alison Kuony; Frederic Michon
Journal:  Invest Ophthalmol Vis Sci       Date:  2022-08-02       Impact factor: 4.925

  2 in total

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