ORPHA:902
Werner syndrome
Also called Adult progeria, WS
- Body system
- Skin diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Adolescent, Adult
- Estimated prevalence
- 1-9 / 1 000 000 (United States)
- Rarity class
- 1-9 / 1 000 000
ORPHA:902 is classified under "Skin diseases" in the Orphanet nomenclature.
Common signs
- Hypogonadism
- Convex nasal ridge
- Cataract
- Abnormal thorax morphology
- Osteoporosis
- Slender build