alpha-1 antitrypsin deficiency

Alpha-1 Antitrypsin Deficiency: Causes, Symptoms & Treatment

Alpha-1 antitrypsin deficiency is a hereditary disease characterized by defective synthesis of alpha-1 antitrypsin in the liver, causing damage to the liver and lungs. Alpha-1-antitrypsin deficiency represents one of the causes of respiratory diseases that are often not recognized or recognized late. What is alpha-1-antitrypsin deficiency? Alpha-1 antitrypsin deficiency is a hereditary disorder that has … Alpha-1 Antitrypsin Deficiency: Causes, Symptoms & Treatment

Hereditary Diseases: Causes, Symptoms & Treatment

Diseases that are “passed from parents to children” are referred to in common parlance as hereditary diseases. Genetic diseases are divided into three groups: chromosomal abnormalities, monogenic diseases, and polygenic inherited diseases. What are inherited diseases? Hereditary diseases are clinical pictures or diseases that arise due to errors in the hereditary dispositions or are newly … Hereditary Diseases: Causes, Symptoms & Treatment

Residual Volume: Function, Role & Diseases

Residual volume is the amount of air that remains as residual air in the lungs and airways even during deep exhalation. It maintains the internal pressure of the alveoli and prevents them from collapsing and becoming irreversibly stuck together. In addition, to a small extent, residual air allows continuity of gas exchange during the pause … Residual Volume: Function, Role & Diseases

Liver Fibrosis: Causes, Symptoms & Treatment

In liver fibrosis, previous disease causes healthy liver tissue to break down and be replaced by collagenous connective tissue. This scarring often forms a transitional stage to cirrhosis. What is liver fibrosis? Fibrosis is the medical term for an increase in connective tissue within an organ. In the case of liver fibrosis, replacement of functional … Liver Fibrosis: Causes, Symptoms & Treatment