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Alpha1Antitrypsin (AAT) Deficiency: A guide to counseling patients from testing to treatmentProvided by Grills PARTS OF THIS BROCHURE WERE ADAPTED FROM THE ALPHA1 FOUNDATION PUBLICATION, Alpha1 Antitrypsin
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To fill out aat deficiency, follow these steps:
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Educate yourself about aat deficiency - learn about the causes, symptoms, and treatment options.
03
Consult with a healthcare professional - it is important to seek medical advice and guidance when dealing with aat deficiency.
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Undergo necessary tests - your healthcare provider may order tests to determine your level of aat deficiency and assess the extent of damage to your lungs and liver.
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Create a treatment plan - work with your healthcare provider to develop a personalized treatment plan that may include medication, pulmonary rehabilitation, and lifestyle changes.
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Follow the prescribed treatment - adhere to the recommended medication regimen, attend scheduled appointments, and make necessary lifestyle modifications.
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Seek support - consider joining support groups or connecting with others who are also dealing with aat deficiency to share experiences and receive emotional support.

Who needs aat deficiency?

01
Aat deficiency is a genetic condition that primarily affects individuals who inherit the abnormal alpha-1 antitrypsin gene from their parents.
02
People who have a family history of aat deficiency, particularly those with parents or siblings affected by the condition, are at a higher risk.
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Individuals with a history of unexplained liver disease, chronic obstructive pulmonary disease (COPD), or early-onset emphysema may also need to be tested for aat deficiency.
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It is important to consult with a healthcare professional to determine the specific risk factors and whether testing for aat deficiency is necessary.
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AAT deficiency is a genetic disorder that may result in lung and liver disease.
Medical professionals and healthcare providers are typically responsible for diagnosing and treating patients with AAT deficiency.
AAT deficiency can be diagnosed through blood tests and genetic testing. Treatment options may include medication and lifestyle changes.
The purpose of diagnosing AAT deficiency is to prevent or manage associated health issues and improve quality of life for affected individuals.
Information to be reported may include genetic test results, symptoms, medical history, and treatment plan.
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