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Ehlers-Danlos Syndrome: Symptoms, Causes Treatment Ehlers-Danlos syndrome is a genetic condition that makes your body’s connective tissue weaker than it should be It commonly affects your skin and joints There’s no cure, but your healthcare provider will help you find treatments to manage your symptoms and prevent potentially dangerous complications
What is EDS? - The Ehlers Danlos Society The Ehlers-Danlos syndromes (EDS) are a group of 13 heritable connective tissue disorders The conditions are caused by genetic changes that affect connective tissue Each type of EDS has its own set of features with distinct diagnostic criteria
What Is Ehlers-Danlos Syndrome (EDS)? Symptoms, and Causes People with EDS may experience increased joint mobility and have stretchy, fragile skin that’s prone to breaking Each case of EDS is different, and there’s no singular cure for the condition
Ehlers-Danlos syndrome - Symptoms and causes - Mayo Clinic Ehlers-Danlos syndrome is a group of inherited disorders that affect your connective tissues — primarily your skin, joints and blood vessel walls Connective tissue is a complex mixture of proteins and other substances that provide strength and elasticity to the underlying structures in your body
Ehlers-Danlos Syndrome - EDS | MedlinePlus There are several types of EDS They can range from mild to life-threatening About 1 in 5,000 people has EDS There is no cure Treatment involves managing symptoms, often with medicines and physical therapy It also includes learning how to protect your joints and prevent injuries
Ehlers–Danlos syndrome - Wikipedia Ehlers–Danlos syndromes (EDS) are a group of 14 genetic connective tissue disorders [7] Symptoms often include loose joints, joint pain, stretchy, velvety skin, and abnormal scar formation [1] These may be noticed at birth or in early childhood [3]
Ehlers-Danlos syndrome (EDS) - Cedars-Sinai EDS is caused by a genetic mutation that can occur in one of eight different genes, based on the type of EDS the patient has People with EDS have a 50 percent chance of passing the condition on to their children Diagnosis of EDS is usually based on symptoms, family medical history and genetic testing
Ehlers-Danlos Syndrome - StatPearls - NCBI Bookshelf Ehlers Danlos syndrome (EDS) is a group of hereditary connective tissue disorders that manifests clinically with skin hyperelasticity, hypermobility of joints, atrophic scarring, and fragility of blood vessels
Ehlers-Danlos Syndrome: Symptoms, Diagnosis, Treatment EDS is named after the two doctors, Ehlers and Danlos, who first described it The syndrome is now known to include 13 different types of connective tissue disorders While all slightly