Keyword Analysis & Research: alpha1


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Frequently Asked Questions

What are the symptoms of Alpha-1?

Alpha 1 -agonists can cause headache, reflex bradycardia, excitability, and restlessness. Because alpha 1 -agonists produce systemic vasoconstriction, the work and oxygen requirements of the heart increase.

How is Alpha-1 inherited?

Alpha-1 Antitrypsin Deficiency (Alpha-1) is a genetic (inherited) condition – it is passed from parents to their children through their genes. Alpha-1 may result in serious lung disease in adults and/or liver disease at any age. For each trait a person inherits, there are usually two genes; one gene comes from each parent.

What are the consequences of Alpha-1?

Alpha-1 may result in serious lung disease in adults and/or liver disease at any age. For each trait a person inherits, there are usually two genes; one gene comes from each parent. People with Alpha-1 have received two abnormal alpha-1 antitrypsin genes. One of these abnormal genes came from their mother and one from their father.

What are the symptoms of alpha-1 antitrypsin deficiency?

Alpha-1 antitrypsin deficiency is a genetic condition that can cause lung and liver damage. Lung symptoms are usually similar to emphysema, including chronic cough, shortness of breath and wheezing. Treatments can reduce your risk of lung damage. Not smoking is the best way to reduce your risk of serious complications.


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