Alpha-1 Anti Trypsin Deficiency
Alpha-1 antitrypsin lack (Alpha1-antitrypsin insufficiency, A1AD, or AATD) is a hereditary issue that causes faulty creation of alpha-1 antitrypsin (A1AT), prompting diminished A1AT movement in the blood and lungs, and affidavit of intemperate irregular A1AT protein in liver cells leading to lung illness and liver infection. Influenced people frequently develop emphysema, which is a lung infection caused by damage to alveoli. Alpha-1 antitrypsin deficiency (A1AD or AATD) is a genetic disorder that may result in lung disease or liver disease. Onset of lung problems is typically between 20 and 50 years old. This may result in shortness of breath, wheezing, or an increased risk of lung infections.
- Pneumothorax
- Bronchiectasis
- Emphysema
- Granulomatosis with polyangiitis
Related Conference of Alpha-1 Anti Trypsin Deficiency
April 21-22, 2025
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October 13-14, 2025
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November 24-25, 2025
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Alpha-1 Anti Trypsin Deficiency Conference Speakers
Recommended Sessions
- Alpha-1 Anti Trypsin Deficiency
- ARDS of Lung Cancer
- Awareness and Prevention of Lung Cancer
- Biomarkers of NSCLC
- Bronchial Adenoma
- Chemotherapy for Lung Cancer
- Classification of Lung Cancer
- Diagnostic Evaluation of Lung Cancer
- Genetic Abnormalities of Lung Cancer
- Immunotherapy for Lung Cancer
- Lung Cancer Surgery
- Lung Disease and Respiratory Health
- Molecular Background of Lung Cancer
- Pediatric Lung Cancer
- Radiotherapy for Lung Cancer
- Risk Factors and Symptoms of Lung Cancer
- Screening of Lung Cancer
- Targeted Therapy for Lung Cancer
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