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As the deficiency of alpha-1 antitrypsin glycoprotein affects the severity of lung disease among patients with Cystic Fibrosis
Author(s) -
CYNTHIA MARA PEREIRA BEZERRA,
Carmen Sílvia Bertuzzo
Publication year - 2016
Publication title -
anais do congresso de iniciação científica da unicamp
Language(s) - English
Resource type - Conference proceedings
ISSN - 2447-5114
DOI - 10.19146/pibic-2016-51997
Subject(s) - cystic fibrosis , alpha 1 antitrypsin deficiency , medicine , glycoprotein , disease , lung , alpha (finance) , lung disease , fibrosis , pathology , gastroenterology , biology , surgery , genetics , construct validity , patient satisfaction
Cystic Fibrosis (CF) is a serious genetic disease, CF is an autosomal recessive genetic disease clinical manifestations can vary being detectable after birth or in adulthood. Basically the defect affects the cells of various organs , which can be presented in different ways in individuals with the disease. With this research can therefore conclude that the alpha-1 antitrypsin deficiency is an aggravating factor for lung disease in people with cystic fibrosis.

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