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Cutis laxa

MONDO:0016175

Cutis laxa (CL) is an inherited or acquired connective tissue disorder characterized by wrinkled, redundant and sagging inelastic skin associated with skeletal and developmental anomalies and, in some cases, with severe systemic involvement. Several different forms of inherited CL have been described, differentiated on the basis of the mode of inheritance and differences in the extent of internal organ involvement, associated anomalies and disease severity.

Also known as: cutis laxa, elastolysis, generalised elastolysis, generalized elastolysis

39 clinical trials for this condition and its sub-types, 37 tagged with Cutis laxa itself.

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Where it sits in the disease tree

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Part of

↑ Integumentary system disorder (4553) ↑ Developmental defect during embryogenesis (1057)

Sub-types of Cutis laxa

Most studied deeper sub-types

Cutis laxa, autosomal recessive, type 1A (1) Autosomal recessive cutis laxa type 2A (0) Autosomal recessive cutis laxa type 2B (0) Autosomal recessive cutis laxa type 2C (0) Autosomal recessive cutis laxa type 2D (0) Cutis laxa, autosomal dominant 1 (0) Cutis laxa, autosomal dominant 2 (0) Cutis laxa, autosomal dominant 3 (0) Cutis laxa, autosomal recessive, type 1B (0) Cutis laxa, autosomal recessive, type 1d (0) Wrinkly skin syndrome (0)
Including sub-types (39) Tagged with Cutis laxa (37)
Trials to join now! 9 Not yet recruiting 12 Not yet finished but already full! 5 Completed 12 Terminated 1
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