Alpha 1 antitrypsin deficiency (AATD) can present with liver dysfunction in individuals from infancy to adulthood, and more infamously with chronic obstructive pulmonary disease COPD), usually when over 30 years of age. Individuals with AATD are also at increased risk for panniculitis (migratory, inflammatory, tender skin nodules which may ulcerate on legs and lower abdomen) and C-ANCA-positive vasculitis (granulomatosis with polyangiitis). For full diagnosis of AATD, testing for the phenotype and genotype is also required.
If you wish to know the level of alpha 1 antitrypsin (ie do you actually have a low level of this protein), this is the test you need. If the level of alpha 1 antitrypsin is within normal limits, no further testing is required.
This confidential blood assay for Alpha 1 anti trypsin serum level is offered at all of the thirty two private clinics across England, Scotland and Wales.
Included in every test request for Alpha 1 antitrypsin genotype are a Doctors Referral, all Phlebotomy fees (your blood is taken at a Private Hospital), all laboratory fees, and our doctor's comments.
Inclusions: analysis for this analyte only.
Special Instructions: Refer to testing laboratories repertoire for vacutainer requirement and testing instructions
Attendance Restrictions: No Special Attendance Restrictions.
Laboratory Notes: Female: 0.6 - 1.29 Male: 0.58 - 1.25
Sample Container: 1x Gold (min 2ml)
Fasting: If fasting is required, it will be explained on your Pathology Passport. 8 hours fasting is sufficient when it is required.