Alpha 1-antitrypsin deficiency other diagnostic studies
Alpha 1-antitrypsin deficiency Microchapters |
Differentiating Alpha 1-antitrypsin deficiency from other Diseases |
---|
Diagnosis |
Treatment |
Case Studies |
Alpha 1-antitrypsin deficiency other diagnostic studies On the Web |
American Roentgen Ray Society Images of Alpha 1-antitrypsin deficiency other diagnostic studies |
FDA on Alpha 1-antitrypsin deficiency other diagnostic studies |
CDC on Alpha 1-antitrypsin deficiency other diagnostic studies |
Alpha 1-antitrypsin deficiency other diagnostic studies in the news |
Blogs on Alpha 1-antitrypsin deficiency other diagnostic studies |
Directions to Hospitals Treating Alpha 1-antitrypsin deficiency |
Risk calculators and risk factors for Alpha 1-antitrypsin deficiency other diagnostic studies |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Please help WikiDoc by adding content here. It's easy! Click here to learn about editing.
Overview
Other Diagnostic Studies
Phenotyping Patients with low or borderline serum levels are tested with phenotyping (serum levels < 100 mg/dL) by isoelectric focusing (IEF) is the most commonly used method to definitively detect the alpha1-antitrypsin phenotype that indicates a risk for AATD. Phenotyping is required to confirm AATD. Do not initiate alpha1-antitrypsin replacement therapy without testing. PiZZ phenotype is responsible for nearly all cases of AATD emphysema and liver disease. PiSZ and PiZ/Null are other phenotypes associated with alpha1-antitrypsin emphysema and liver disease. PiNull/Null is not associated with liver disease but is associated with alpha1-antitrypsin deficiency emphysema. Genotyping uses DNA extracted from circulating mononuclear blood cells that utilizes DNA amplification techniques with melt-curve analysis.