Cutis laxa. Cutis laxa

In Pagon RA, Bird TD, Dolan CR, et al Accessed August 26, 2021
The benign autosomal recessive form also causes intellectual disability and joint laxity For all patients whose precise type has not yet been identified, this is an extraordinary chance
Rheumatoid arthritis• Case Reports in Dermatology References [ ]• The skin normally has fine wrinkles, is loose, has a tendency to fold, and is very silky to the touch
You can be tested […]
Contact a health care provider if you have questions about your health In: Bissonnette B, Luginbuehl I, Marciniak B, Dalens BJ
Pulmonary manifestations such as emphysema and pulmonary fibrosis• Gastrointestinal tract hernias and diverticula are common Variants in the genes described above account for only a small percentage of all cases of cutis laxa
Congenital cutis laxa, a rare syndrome with marked skin laxity and pulmonary and cardiovascular compromise, is due to defective elastic fiber formation Genetic counseling: FBLN5-related cutis laxa can be inherited in an autosomal recessive or less commonly autosomal dominant manner
The X-linked form of cutis laxa, occipital horn syndrome, is caused by variants in the gene Yes, Cutis Laxa Internationale is a support group based in Saint-Cergues, France
Other symptoms are low muscle tone, growth delays, and loose joints Most cases of cutis laxa are inherited as an autosomal recessive trait