Autosomal recessive cutis laxa type 1

Autosomal recessive cutis laxa, type 1 (ARCL1) is a generalized connective tissue disorder characterized by the association of wrinkled, redundant and sagging inelastic skin with severe systemic manifestations (lung atelectesias and emphysema, vascular anomalies, and gastrointestinal and genitourinary tract diverticuli).

Also known as: ARCL1, autosomal recessive cutis laxa type 1, autosomal recessive cutis laxa with severe systemic involvement, autosomal recessive cutis laxa, pulmonary emphysema type, autosomal recessive cutis laxa type I, cutis laxa, autosomal recessive type 1, cutis laxa, type 1

5 clinical trials for this condition and its sub-types.