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

PUBMED FOR HANDHELDS

Search MEDLINE/PubMed

  • Title: [Hereditary angioedema: pathogenesis, ophthalmological significance, diagnosis and therapy (author's transl)].
    Author: Daxecker F.
    Journal: Klin Monbl Augenheilkd; 1980 Sep; 177(3):390-3. PubMed ID: 7453075.
    Abstract:
    Hereditary angioedema is caused by a deficiency of the C 1 esterase inhibitor (a component of complement). It is manifested by attacks of swelling of the extremities, face, eyelids, trunk, respiratory tract or abdominal viscera. The ophthalmological significance, diagnosis, symptoms and treatment of the condition are discussed.
    [Abstract] [Full Text] [Related] [New Search]