Literature DB >> 962658

Hereditary congenital alacrima.

B J Mondino, S I Brown.   

Abstract

We describe a family with markedly deficient lacrimation from infancy and punctate corneal epithelial erosions. An autosomal dominant inheritance pattern is suggested. A hypoplasia of the lacrimal gland in this family was suggested by pharmacologic testing and by histopathologic examination of the lacrimal gland of the proposita. The family investigated in this report represents the first instance of hereditary congenital alacrima without associated ocular or adnexal abnormalities and apart from systemic disorders such as the Riley-Day syndrome and anhidrotic ectodermal dysplasia.

Entities:  

Mesh:

Substances:

Year:  1976        PMID: 962658     DOI: 10.1001/archopht.1976.03910040312003

Source DB:  PubMed          Journal:  Arch Ophthalmol        ISSN: 0003-9950


  3 in total

1.  LADD syndrome: report of new cases and review of the clinical spectrum.

Authors:  H R Wiedemann; J Drescher
Journal:  Eur J Pediatr       Date:  1986-04       Impact factor: 3.183

2.  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 3.  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

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.