ORPHA:90186
Meige disease
Also called Hereditary lymphedema type II, Meige lymphedema
- Body system
- Skin diseases
- Inheritance pattern
- Not applicable
- Typical age of onset
- Adolescent, Childhood
- Estimated prevalence
- Unknown (Worldwide)
- Rarity class
- Unknown
ORPHA:90186 is classified under "Skin diseases" in the Orphanet nomenclature.
Common signs
- Lymphedema
- Atypical scarring of skin
- Recurrent skin infections
- Lymph node hypoplasia
- Absence of lymph node germinal center
- Predominantly lower limb lymphedema