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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.

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Sub-types

Arterial tortuosity syndrome (1) Autosomal recessive cutis laxa type 1 (1) Cutis laxa, autosomal recessive, type 1A (1) Occipital horn syndrome (1) Acquired cutis laxa (0) ALDH18A1-related de Barsy syndrome (0) Arterial tortuosity-bone fragility syndrome (0) Autosomal dominant cutis laxa (0) Autosomal recessive cutis laxa type 2 (0) 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 2, classic type (0) Autosomal recessive cutis laxa type 2D (0) Craniofaciofrontodigital syndrome (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)

Broader categories

Disease (680) Human disease (14) Developmental defect during embryogenesis (8) Disease by body system or component (0) Disease by developmental or physiological process (0) Disorder of development or morphogenesis (0) Integumentary system disorder (0)
Trials to join now! 9 Not yet recruiting 13 Not yet finished but already full! 4 Completed 12 Terminated 1
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