These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Search MEDLINE/PubMed


  • Title: Autosomal dominant typical coloboma associated with unilateral pseudoptosis, myopia and cataract.
    Author: Porges Y.
    Journal: Cent Afr J Med; 1995 Aug; 41(8):255-7. PubMed ID: 7585914.
    Abstract:
    Ocular coloboma is considered to be hereditary ocular malformation which can manifest itself in various conditions ranging from iris defect to rudimentary cystic eye globe. We describe a three generation family affected by autosomal dominant typical coloboma, unilateral pseudoptosis, myopia and cataract. Correction of refractive errors improved their visual performance and prevented amblyopia. Genetic consultation was given in order to prevent blindness. We recommend a multidisciplinary approach regarding management of colobomatous patients.
    [Abstract] [Full Text] [Related] [New Search]