Cutis laxa
Web Cutis laxa CL is a group of rare diseases of connective tissue characterized by redundant skin with loss of elasticity and premature aging. Cutis laxa is also known as generalised elastolysis.
Web Cutis laxa is the general name for a group of rare disorders that affects your connective tissue.
. Cutis laxa is estimated to affect 1 in 1000000 individuals in the general population. Three major groups are individualized based on the mode of inheritance. Cutis laxa can also affect connective tissue in other parts of the body including the heart blood vessels joints intestines and lungs.
Web Cutis Laxa CL is a rare disorder of connective tissue that affects only about 400 families worldwide or 1 in every 2000000 babies. Web Cutis laxa is associated with deficient or absent elastin fibers in the extracellular matrix. Web Cutis laxa Latin for loose or lax skin is a rare inherited or acquired connective tissue disorder characterised by loosely hanging skin that lacks any elasticity.
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1 Heritable forms have variable transmissions and clinical expressions. Web Cutis laxa or elastolysis is a rare inherited or acquired connective-tissue disorder in which the skin becomes inelastic and hangs loosely in folds. The skin often hangs in loose folds causing the face and other parts of the body to have a droopy appearance.
The disorder has been reported in approximately 400 families worldwide. This can be related to decreased elastin synthesis or structural defects in the extracellular matrix. Generally cutis laxa is characterized by saggy loose wrinkly and inelastic skin especially around the face neck arms legs and torso.
Web Cutis laxa is a rare disorder that affects males and females in equal numbers. This tissue gives your muscles joints skin and organs structure. Web Cutis laxa is a disorder of connective tissue which is the tissue that provides structure and strength to the muscles joints organs and skin.
Autosomal dominant CL autosomal recessive CL and. Patients develop a prematurely aged. Web Cutis Laxa is a rare disorder that causes a defect or an insufficiency of the bodys connective tissue affecting the normal structural framework of the skin muscles joints and sometimes internal organs.
Connective tissue also referred to as the extracellular matrix provides the structural framework for many parts of the body including skin muscles joints blood vessels and even internal organs. Most cases are inherited but some are acquired which means they do not appear to be caused by genetic variations. Most types of cutis laxa.
Cutis laxa may be caused by mutations in the genes. Web Cutis laxa is a connective tissue disorder characterized by skin that is sagging and not stretchy. ELN ATP6V0A2 ATP7A FBLN4 FBLN5 and PYCR1.
The way in which the condition presents itself is different according to how it is inherited or acquired.
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