autosomal recessive cutis laxa type 2
Findings
No curated finding names autosomal recessive cutis laxa type 2 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A spectrum of connective tissue disorders characterized by the association of wrinkled, redundant and sagging inelastic skin with growth and developmental delay, and skeletal anomalies. The spectrum ranges from patients with classic ARCL2 (ARCL, Debre) type) to patients with a milder form of the disease, wrinkled skin syndrome (WSS).
Definition from the Mondo Disease Ontology (MONDO:0019573), read 2026-09-29. CC BY 4.0.
Features
1 feature
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, hp/releases/2026-09-01.
- Reduced bone mineral densityMondoHP:0004349
Where it sits
Other names
2 names
Resolves to: autosomal recessive cutis laxa type 2
- Also called
- ARCL2cutis laxa with joint laxity and developmental delay