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- Alpha-1 Antitrypsin Deficiency: Causes, Symptoms Treatment
What is Alpha-1 antitrypsin deficiency? Alpha-1 antitrypsin deficiency (sometimes just called “Alpha-1”) is an inherited genetic disorder that causes low levels of a protein (AAT) that protects your lungs Alpha-1 increases your risk of developing certain diseases, including emphysema (damaged air sacs in your lungs), cirrhosis (liver scarring) and panniculitis (an uncommon skin condition
- Alpha-1 Antitrypsin Deficiency - StatPearls - NCBI Bookshelf
Alpha-1 antitrypsin (AAT) deficiency is a genetically inherited disorder often unrecognized in clinical practice It results in the impaired production of alpha-1 antitrypsin protein, which plays a role in protecting the body from neutrophil elastase, an enzyme released by white blood cells during infection Due to defective protein production, there is reduced activity of AAT in the blood and
- Alpha-1 antitrypsin deficiency - Wikipedia
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 [1][2] Complications may include chronic obstructive pulmonary disease (COPD), cirrhosis, neonatal jaundice, or
- Alpha-1 Antitrypsin (AAT) Deficiency - WebMD
Learn about the causes, symptoms, and treatment for alpha-1 antitrypsin (AAT) deficiency, along with questions for your doctor and tips for living with it
- Alpha-1 antitrypsin deficiency: MedlinePlus Genetics
Alpha-1 antitrypsin deficiency is an inherited disorder that may cause lung disease and liver disease Explore symptoms, inheritance, genetics of this condition
- What is Alpha-1? Learn More Here - Alpha-1 Foundation
Learn about Alpha-1 Antitrypsin Deficiency, its causes, symptoms, and available resources to improve quality of life
- Learn About Alpha-1 Antitrypsin Deficiency - American Lung Association
In alpha-1 antitrypsin deficiency, the body’s normal production of the AAT protein is impaired, resulting in the destruction of sensitive lung tissue Learn more about what causes this rare condition
- What Is Alpha-1 Antitrypsin Deficiency? - American Thoracic Society
What Is Alpha-1 Antitrypsin Deficiency? Alpha-1 antitrypsin deficiency is a genetic condition that decreases lung protection resulting in an inherited form of emphysema (em-fuh-ZEE-muh) People with the condition, also known as AAT Deficiency or alpha-1 antitrypsin deficiency, do not have enough of a protein called alpha-1 antitrypsin (AAT) in their blood This protein is made in the liver
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