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: Familial occurrence of congenital pulmonary lymphangiectasis. Genetic implications.
    Author: Scott-Emuakpor AB, Warren ST, Kapur S, Quiachon EB, Higgins JV.
    Journal: Am J Dis Child; 1981 Jun; 135(6):532-4. PubMed ID: 7234788.
    Abstract:
    Congenital pulmonary lymphangiectasis (CPL) is a rare, generalized disease of the lung, consisting of lymphatic cysts in the subpleural and interlobular connective tissue. This disorder typically manifests a clinical picture of acute respiratory distress with cyanosis shortly after birth, with death occurring in the neonatal period. Several cases of this disorder have been described in the literature, but there has been no family with more than one affected child. We report the first instance, to our knowledge, of familial cases of CPL, which raises an important question regarding a possible genetic component in this disorder. The implications of this are discussed.
    [Abstract] [Full Text] [Related] [New Search]