Cutis laxa
MONDO:0016175Cutis 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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Browse by category →Sub-types of Cutis laxa
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Inherited cutis laxa 0 trials · 2 incl. sub-types
14 sub-types
- Arterial tortuosity syndrome 1 trial
- Autosomal recessive cutis laxa type 1 1 trial Sub-types →
- Occipital horn syndrome 1 trial
- ALDH18A1-related de Barsy syndrome 0 trials
- PYCR1-related de Barsy syndrome 0 trials
- RIN2 syndrome 0 trials
- Arterial tortuosity-bone fragility syndrome 0 trials
- Autosomal dominant cutis laxa 0 trials Sub-types →
- Autosomal recessive cutis laxa type 2 0 trials Sub-types →
- Autosomal recessive cutis laxa type 2, classic type 0 trials
- Craniofaciofrontodigital syndrome 0 trials
- Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies 0 trials
- Cutis laxa, autosomal recessive, type 2E 0 trials
- Geroderma osteodysplastica 0 trials
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Acquired cutis laxa 0 trials