Cutis laxa

Below you will find more information about Cutis laxa from Medigest. If you believe that you are suffering from any of the symptoms of Cutis laxa it is important that you obtain an accurate diagnosis from a medical professional to ensure that you obtain the correct medication or treatment for your condition. There are medical conditions that carry similar symptoms associated with Cutis laxa and therefore the information provided by Medigest is offered as a guideline only and should never be used in preference to seeking professional medical advice. The information relating to Cutis laxa comes from a third party source and Medigest will not be held liable for any inaccuracies relating to the information shown.


Cutis laxa (CL) is an extremely rare disease that can either be acquired or inherited disorder of the connective tissue. This is characterized by marked inelasticity of the skin that usually hangs in folds. In both inherited and acquired cutis laxa, the internal organs may also be affected.


There are actually no definite laboratory findings for cutis laxa. Chest radiography may be also be done to check for possible pulmonary involvement.


There are no treatments that currently exist to prevent the progression of the disease. Surgical procedures may be conducted to correct skin folds, and facial defects.

Symptoms and Signs

Primary symptoms include abnormally loss skin that hangs in fold and inelastic, skin fragility, prone to bruises, large bowels due to the its effect on the gastrointestinal tract along with emphysema, congestive heart failure, cardiomegaly, and even osteoporosis.


The underlying cause of cutis laxa is still not known and probably variable. Some theories include low lysyl oxidase activity, abnormal copper metabolism/copper deficiency, decreased elastin gene expression, increased elastase activity and immune-mediated mechanisms. Surgical Care

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