Witryna4 sty 2012 · Alpha-1 antitrypsin deficiency (AATD) is an inherited condition that causes low levels of, or no, alpha-1 antitrypsin (AAT) in the blood. AATD occurs in approximately 1 in 2,500 individuals. This … WitrynaLung Disease. Alpha-1 Antitrypsin Deficiency (Alpha-1) is a genetic condition passed from parents to their children through their genes. Genes are the code, or instructions, to our body’s cells that give us blue eyes, black hair, and so on. We inherit our genes from our parents – half from each parent – so we say our skin color or other ...
About Alpha-1 Antitrypsin Deficiency - Genome.gov
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Alport syndrome - Wikipedia
WitrynaAlport syndrome. Alport syndrome is a genetic disorder [1] affecting around 1 in 5,000-10,000 children, [2] characterized by glomerulonephritis, end-stage kidney disease, and hearing loss. [3] Alport syndrome can also affect the eyes, though the changes do not usually affect vision, except when changes to the lens occur in later life. Witryna1 gru 2024 · In allergic asthma, the attacks occur when substances known as allergens are inhaled, causing an allergic reaction. Allergens are harmless substances that the body's immune system mistakenly reacts to as though they are harmful. Common allergens include pollen, dust, animal dander, and mold. The immune response leads … WitrynaSigns and Symptoms of Rare/Genetic Lung Disease. Each rare lung disease is different, and they can be mild or severe; however, many share these common signs and symptoms: Poor growth or weight gain. Fast and/or labored breathing. Chronic or recurrent cough, wheeze, or crackling sounds during breathing. Shortness of breath … makhadzi ft mr brown songs