AUTOIMMUNE BULLOUS DERMATOSES PROFILE IgG (S331) - Delhi
OUTSOURCE
|
Radiology
Also Known As:
Bullous autoimmune dermatoses belong to the organ-specific autoimmune diseases. They are characterised by the formation of autoantibodies against structural proteins of the skin. These structural proteins establish the cell-to-cell contact in keratinocytes within the epidermis and the adhesion of the epidermis to the dermis. Bullous autoimmune dermatoses are divided into four main groups based on their target antigens and the localisation of the blisters: Pemphigoid diseases, Pemphigus diseases, including Paraneoplastic Pemphigus, Epidermolysis bullosa acquisita (EBA) and Dermatitis herpetiformis (DH). In Pemphigus diseases the blisters are formed intra-epidermally, whereas in Pemphigoid diseases, EBA and DH they occur sub-epidermally.
-
Home Collection: Not Available
-
Reports Available: 2 Days
TAT Policy
The Turnaround Time (TAT) for a test depends on the following factors:
- Registration date and time
- Type of scan or test
- Scan time or sample collection time
Please note that in uncommon circumstances, TAT may be delayed due to the complexity of the test or reasons beyond our control. You will be informed about the estimated TAT at the time of registration or after completion of the test.
