Alpha-1 Antitrypsin Deficiency

Alpha-1 antitrypsin deficiency is a hereditary disorder in which the body produces a low amount of a protein that protects the lungs and the liver from damage.

How can it manifest? When this protection is lacking, respiratory problems such as difficulty breathing or persistent cough may appear, and in some cases liver abnormalities.

When to seek care? Respiratory symptoms that appear at an early age or without an evident cause, especially with a family history, are worth investigating.

Which specialist treats it? The pulmonologist is the indicated professional to assess the respiratory component and guide follow-up. If you notice difficulty breathing repeatedly, reach out to them so that they can thoroughly evaluate your situation.