Please use one of the following formats to cite this article in your essay, paper or report. Physicians should be able to differentiate the less severe form of jhs from the vascular ehlersdanlos syndrome, to diagnose it before the. Jul 09, 2014 ehlers danlos syndrome is a rare clinical condition caused by a genetic change that results in the formation of structurally or functionally altered collagen. People who have ehlers danlos syndrome, vascular type, often share distinctive facial features of a thin nose, thin upper lip, small earlobes and prominent eyes. Give your medical professionals a hand with this 2017 ehlers danlos classification handout project echo information brochure pdf to inform your health professionals about the eds project echo program. Defects in connective tissues cause the signs and symptoms of these conditions, which range from mildly loose joints to lifethreatening complications. Ehlers danlos syndrome is a group of disorders that affect connective tissues, which are tissues that support the skin, bones, blood vessels, and other organs. Ehlersdanlos syndrome, in short, eds refers to a bunch of hereditary connective tissue disorders. Download as pptx, pdf, txt or read online from scribd. The ehlers danlos society is a global community of patients, caregivers, health care professionals, and supporters, dedicated to saving and improving the lives of those affected by the ehlers danlos syndromes, hypermobility spectrum disorders, and related conditions. Ehlersdanlos syndrome associated with cardiomyopathy. Give your medical professionals a hand with this 2017 ehlersdanlos classification handout project echo information brochure pdf to inform your health professionals about the eds project echo program.
Ehlers danlos syndrome eds is a heterogeneous group of inherited connective tissue disorders, caused by mutations in the genes that codify fibrillar collagen or the enzymes implicated in modifying posttranslational collagen. Oct, 2017 some people with ehlers danlos syndrome will have overly flexible joints, but few or none of the skin symptoms. Mar 01, 2017 the cover image, by brad tinkle et al. Apr 20, 2012 ehlersdanlos syndrome eds is a heterogeneous group of heritable connective tissue disorders whose primary clinical features include soft and extensible skin, articular hypermobility and tissue fragility.
Ehlersdanlos syndrome is a group of genetic disorders that affects the bodys connective tissue. Ehlers danlos syndrome and osteoporosis article pdf available in annals of the rheumatic diseases 5312. Defects in connective tissues cause the signs and symptoms of ehlers danlos syndrome, which vary from mildly loose joints to lifethreatening complications. Este sitio web ha sido creado y es administrado por alejandra guasp, lic. However, the genetic study to confirm the diagnosis was not done. Ehlers danlos syndrome is a group of disorders that affect connective tissues supporting the skin, bones, blood vessels, and many other organs and tissues. Many people with eds experience other symptoms, such as chronic pain, fatigue, easy bruising, poor wound healing and abnormal scarring. Ehlersdanlos syndromes eds are a group of genetic connective tissue disorders. These can be noticed at birth or in early childhood. O colageno no tecido conjuntivo ajuda a resistir a deformacao dos tecidos. Its key characteristics are stretchy skin and flexible joints. Symptoms may include loose joints, joint pain, stretchy velvety skin, and abnormal scar formation. Ehlersdanlos syndrome symptoms and causes mayo clinic. The clinical manifestations are varied, being the most obvious skin hypermotility and increased.