ORPHA:90350
Autosomal recessive cutis laxa type 2
Also called ARCL2, Cutis laxa with joint laxity and developmental delay
- Body system
- Skin diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Infancy, Neonatal
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:90350 is classified under "Skin diseases" in the Orphanet nomenclature.