Acquired C1 esterase inhibitor deficiency
Acquired C1 esterase inhibitor deficiency presents with symptoms indistinguishable from hereditary angioedema, but generally with onset after the fourth decade of life.[1]:153
| Acquired C1 esterase inhibitor deficiency | |
|---|---|
| Other names | Acquired angioedema |
| Specialty | Hematology |
C4 levels are low and C3 levels are normal.[2]
See also
- Hereditary Angioedema
- Wheal response
- Urticaria
- Skin lesion
- List of cutaneous conditions
References
- James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0-7216-2921-0.
- Markovic SN, Inwards DJ, Frigas EA, Phyliky RP (January 2000). "Acquired C1 esterase inhibitor deficiency". Ann. Intern. Med. 132 (2): 144–50. doi:10.7326/0003-4819-132-2-200001180-00009. PMID 10644276.
External links
| Classification | |
|---|---|
| External resources |
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