ORPHA:2833
Stiff skin syndrome
- Body system
- Skin diseases
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- Childhood, Infancy, Neonatal
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:2833 is classified under "Skin diseases" in the Orphanet nomenclature.
Common signs
- Thickened skin
- Limitation of joint mobility
- Lack of skin elasticity
- Hyperpigmentation of the skin
- Hypertrichosis
- Sensorineural hearing impairment