Bronchiectasis and homozygous (P1ZZ) alpha 1-antitrypsin deficiency in a young man

Rodriguez-Cintron, W; Guntupalli, K; Fraire, A E
April 1995
Thorax;Apr1995, Vol. 50 Issue 4, p424
Academic Journal
No abstract available.


Related Articles

  • Alpha-1 Antirtypsin Deficiency, Emphysema, and Cirrhosis in an Adult. Cohen, Kenneth L.; Rubin, Peter E.; Echevarria, Rene A.; Sharp, Harvey L.; Teague, Perry O. // Annals of Internal Medicine;Feb73, Vol. 78 Issue 2, p227 

    Provides information on a study which described the association of a homozygous deficiency of serum alpha-1 antitrypsin with pulmonary emphysema in children. Details of a case report of a middle-aged man with pulmonary emphysema and homozygous alpha-1 antitrypsin deficiency; Characteristics of...

  • Predictive value of alpha-1 antitrypsin level for Z mutation detection in chronic obstructive pulmonary disease. Serapinas, Danielius // Biologija;2013, Vol. 59 Issue 4, p341 

    Alpha1-antitrypsin (AAT) deficiency is an under-diagnosed condition in patients with chronic obstructive pulmonary disease (COPD). The aim of our study was to evaluate predictive value of quantitative methods of alpha-1 antitrypsin for Z mutation detection in patients with chronic obstructive...

  • Alpha[sub1]-Antitrypsin. Freeman, H. J.; Weinstein, W. M.; Shnitka, T. K.; Crockford, P. M.; Herbert, F. A. // Annals of Internal Medicine;Jul76, Vol. 85 Issue 1, p73 

    Presents a case report on a patient with homozygous ZZ alpha 1-antitrypsin deficiency and pancreatic fibrosis. Pathophysiology of both diseases; Medical history of the patient; Clinical manifestations and treatment.

  • Alpha-1-antitrypsin deficiency and a pleural shadow. Ho, Timothy B. L.; Massouh, Hassan; Knight, R. K. // Journal of the Royal Society of Medicine;Jul1999, Vol. 92 Issue 7, p364 

    The article describes the case of a 72-year-old woman who was diagnosed with alpha-1-antitrypsin deficiency associated emphysema and reversible pleural changes ascribed to a hemothorax in the setting of an acute infection. She was treated with intravenous antibiotics and oral prednisolone and...

  • University College London Collaboration Aims to Treat Alpha-1-Antitrypsin Deficiency (Case study). Lomas, David // International Labmate;Apr2014, Vol. 39 Issue 3, p52 

    The article presents a case study of treating Alpha-1 antitrypsin deficiency.

  • Alpha-antitrypsin deficiency and liver disease.  // British Medical Journal (Clinical Research Edition);9/26/1981, Vol. 283 Issue 6295, p807 

    Examines the genetics of alpha-antitrypsin deficiency and liver disease in Sweden. Role of alpha-antitrypsin as a serum protease inhibitor; Identification on the autosomal codominant pattern of alleles; Association between alpha-antitrypsin and childhood cirrhosis.

  • Dalteparin sodium.  // Reactions Weekly;12/15/2012, Issue 1432, p20 

    The article describes the case of a 52-year-old man, diagnosed with alpha-1 antitrypsin deficiency (AATD), who developed toxic and cholestatic hepatitis while under dalteparin sodium treatment regimen.

  • Alteration in Distribution of Pulmonary Blood Flow. Levine, Barry W.; Talamo, Richard C.; Shannon, Daniel C.; Kazemi, Homayoun // Annals of Internal Medicine;Sep70, Vol. 73 Issue 3, p397 

    Provides information on a study that conducted a physiological evaluation of lung function including distribution of perfusion and ventilation with xenon-133 in seven subjects, ages nine to 49 years, with homozygous alpha[sub1]-antitrypsin deficiency. Methodology of the study; Results and...

  • Deficiency of Alpha-1 Antitrypsin. Alper, Chester A. // Annals of Internal Medicine;Feb73, Vol. 78 Issue 2, p298 

    Discusses the physiological effects of genetic deficiency of alpha-1 antitrypsin. List of diseases associated with the alpha-1 antitrypsin deficiency; Types of proteolytic enzymes; Inhalant which hastens the lung disease of genetically susceptible individuals.

  • Adult Liver Disease in SZ Phenotype Alpha--1--Antitrypsin Deficiency. Palmer, Philip E.; Gherardi, Gherardo J.; Baldwin, Joseph M.; Wolfe, Hubert J. // Annals of Internal Medicine;Jan78, Vol. 88 Issue 1, p59 

    Reports on the association of liver disease with alpha-1-antitrypsin deficiency. Detection of periodic acid-Schiff-positive globules within periportal hepatocytes; Presence of characteristic alpha-1-antitrypsin globules; Tissue diagnosis of alpha-1-antitrypsin deficiency liver disease.


Read the Article


Sign out of this library

Other Topics