You are visiting the website of the Patients’ Support Group “Cutis Laxa Internationale” .
Our pages are dedicated to all those who are concerned by this rare genetic disorder Cutis Laxa:
sufferers, sufferers’ families, but also health professionnals and all people interested in rare disorders issues.
We do not accept any advertising nor receive any funds from advertisements.
You want to come in contact with (other) patients? If you are a patient, patient’s parents, doctor or a researcher,
we invite you to join our support group on facebook