Alpha-1 Antitrypsin Deficiency

Category: Genetic Disorders / Metabolic Disorders

Alpha-1 Antitrypsin Deficiency (AATD) is a genetic disorder that causes a deficiency of the alpha-1 antitrypsin protein, primarily leading to lung disease (emphysema) and liver disease.

Global Prevalence

Estimated 1 in 3,000 to 5,000 individuals of European descent, but often underdiagnosed. (Source: Alpha-1 Foundation)

Medical Breakthroughs

Discover the latest clinical trials and treatments for Alpha-1 Antitrypsin Deficiency on JourneyForHealth.

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