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  2. Alpha-1 antitrypsin deficiency - Wikipedia

    en.wikipedia.org/wiki/Alpha-1_antitrypsin_deficiency

    Alpha-1 antitrypsin deficiency (A1AD or AATD) is a genetic disorder that may result in lung disease or liver disease. [1] Onset of lung problems is typically between 20 and 50 years of age. [ 1 ] This may result in shortness of breath , wheezing , or an increased risk of lung infections .

  3. Alpha-1 antitrypsin - Wikipedia

    en.wikipedia.org/wiki/Alpha-1_antitrypsin

    Alpha-1 antitrypsin or α 1-antitrypsin (A1AT, α 1 AT, A1A, or AAT) is a protein belonging to the serpin superfamily. It is encoded in humans by the SERPINA1 gene.A protease inhibitor, it is also known as alpha 1 –proteinase inhibitor (A1PI) or alpha 1-antiproteinase (A1AP) because it inhibits various proteases (not just trypsin). [5]

  4. Alpha 1-antichymotrypsin - Wikipedia

    en.wikipedia.org/wiki/Alpha_1-antichymotrypsin

    20714 Ensembl ENSG00000196136 ENSMUSG00000058207 UniProt P01011 P07759 RefSeq (mRNA) NM_001085 NM_011458 RefSeq (protein) NP_001076 NP_035588 Location (UCSC) Chr 14: 94.61 – 94.62 Mb Chr 12: 104.3 – 104.31 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Alpha 1-antichymotrypsin (symbol α 1 AC, A1AC, or a1ACT) is an alpha globulin glycoprotein that is a member of the serpin ...

  5. Emphysema - Wikipedia

    en.wikipedia.org/wiki/Emphysema

    Alpha-1 antitrypsin deficiency is a genetic risk factor that may lead to the condition presenting earlier. [9] When associated with significant airflow limitation, emphysema is a major subtype of chronic obstructive pulmonary disease (COPD), a progressive lung disease characterized by long-term breathing problems and poor airflow.

  6. Cirrhosis - Wikipedia

    en.wikipedia.org/wiki/Cirrhosis

    Alpha-1 antitrypsin deficiency is an autosomal co-dominant disorder of low levels of the enzyme alpha-1 antitrypsin [32] Cardiac cirrhosis is due to chronic right-sided heart failure, which leads to liver congestion [32] Galactosemia [57] Glycogen storage disease type IV [44] Cystic fibrosis [32]

  7. Liver disease - Wikipedia

    en.wikipedia.org/wiki/Liver_disease

    Liver damage is also a clinical feature of alpha 1-antitrypsin deficiency [11] and glycogen storage disease type II. [12] In transthyretin-related hereditary amyloidosis, the liver produces a mutated transthyretin protein which has severe neurodegenerative or cardiopathic effects. Liver transplantation can be curative. [13]

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  9. Protease inhibitor (biology) - Wikipedia

    en.wikipedia.org/wiki/Protease_inhibitor_(biology)

    In medicine, protease inhibitor is often used interchangeably with alpha 1-antitrypsin (A1AT, which is abbreviated PI for this reason). [3] A1AT is indeed the protease inhibitor most often involved in disease, namely in alpha-1 antitrypsin deficiency.

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