ORPHA:220402
Limited cutaneous systemic sclerosis
Also called Limited cutaneous systemic scleroderma
- Body system
- Skin diseases
- Inheritance pattern
- Multigenic/multifactorial, Not applicable
- Typical age of onset
- Adult
- Estimated prevalence
- Not documented in Orphadata
- Rarity class
- Not documented in Orphadata
ORPHA:220402 is classified under "Skin diseases" in the Orphanet nomenclature.
Common signs
- Abnormality of the skin
- Abnormality of skin pigmentation
- Hypopigmented skin patches
- Autoimmunity
- Narrow foramen obturatorium
- Dysphagia