Alpha 1 Antitrypsin Deficiency & COPD
Alpha-1 antitrypsin deficiency is a genetic disorder that is passed on in families and affects the lungs, liver and skin. When this condition affects the lungs, it causes COPD. There is no cure, but treatment can help people with Alpha-1 antitrypsin deficiency manage their symptoms and live a better life. The preliminary symptoms are shortness of breath following mild activity, reduced ability to exercise, and wheezing. Other signs and symptoms include unintentional weight loss, recurring respiratory infections, fatigue, and rapid heartbeat upon standing. Affected individuals often develop emphysema, which is a lung disease caused by damage to the small air sacs in the lungs. Alpha-1 antitrypsin deficiency accounts for 1 to 2% of all cases of chronic obstructive pulmonary disease.
Related Conference of Alpha 1 Antitrypsin Deficiency & COPD
15th International Conference on Pulmonary & Respiratory Medicine
4th International Conference on Tuberculosis, Lung Health and Respiratory Diseases
Alpha 1 Antitrypsin Deficiency & COPD Conference Speakers
Recommended Sessions
- Asthma
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- Alpha 1 Antitrypsin Deficiency & COPD
- Cardiopulmonary Disorders
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- Covid19 Vaccine and Lung Immunopathology
- Cystic Fibrosis
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- Diagnosis and Treatment of COPD
- Digital Health in Respiratory Care
- Effect of COVID-19 on Lungs
- Genetic risk factor of COPD
- Idiopathic Pulmonary Fibrosis
- Innate Immunity and Lung Fibrosis
- Investigational Drugs and Other Therapies in the treatment of Respiratory Disease
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- Pulmonary Rehabilitation
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- Severe Acute Respiratory Syndrome (SARS)
- Sleep apnea
- Tuberculosis
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