ORPHA:901
Wells syndrome
Also called Eosinophilic cellulitis
- Body system
- Skin diseases
- Inheritance pattern
- Not applicable
- Typical age of onset
- Adult
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:901 is classified under "Skin diseases" in the Orphanet nomenclature.
Common signs
- Pruritus
- Cellulitis
- Edema
- Increased total eosinophil count
- Abnormal blistering of the skin
- Skin vesicle