ORPHA:90348
Autosomal dominant cutis laxa
Also called ADCL
- Body system
- Skin diseases
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- Infancy, Neonatal
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:90348 is classified under "Skin diseases" in the Orphanet nomenclature.
Common signs
- Cutis laxa
- Hyperextensible skin
- Redundant skin
- Increased number of skin folds
- Fragmented elastic fibers in the dermis
- Premature skin wrinkling