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- 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 - Diagnosis and treatment - Mayo Clinic
Extremely loose joints, fragile or stretchy skin, and a family history of Ehlers-Danlos syndrome are often enough to make a diagnosis Genetic tests on a sample of your blood can confirm the diagnosis in rarer forms of Ehlers-Danlos syndrome and help rule out other problems
- Síndrome de Ehlers-Danlos - Síntomas y causas - Mayo Clinic
El síndrome de Ehlers-Danlos es un conjunto de trastornos heredados que afectan los tejidos conectivos (principalmente la piel, las articulaciones y las paredes de los vasos sanguíneos) El tejido conectivo es una mezcla compleja de proteínas y otras sustancias que aportan resistencia y elasticidad a las estructuras subyacentes del cuerpo
- Physical Therapy and Ehlers-Danlos Syndromes - Mayo Clinic Connect
There are many modalities patients can choose from for treatment of hypermobile Ehlers-Danlos Syndrome (hEDS) and Hypermobility Spectrum Disorder (HSD) Overarching all of them, is the positive effect of Physical Therapy (PT) and Occupational Therapy (OT)
- Ehlers-Danlos syndromes and Aortic Dilatation: What You Need to Know
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- Ehlers-Danlos syndrome care at Mayo Clinic
There are many different types of Ehlers-Danlos syndrome and the symptoms can overlap Mayo Clinic physicians have extensive expertise in the condition, so they can quickly determine a precise diagnosis and treatment plan
- 埃勒斯-当洛斯综合征 - 症状与病因 - 妙佑医疗国际
病因 不同类型的埃勒斯-当洛斯综合征与各种遗传病因有关，其中部分基因具有遗传性，可从父母遗传给子女。如果您患有最常见的类型（高可动性埃勒斯-当洛斯综合征），则有 50% 的可能性会将此基因遗传给子女。
- EDS and POTS - Mayo Clinic Connect
Many patients with hypermobility spectrum disorder (HSD) and hypermobile EDS (hEDS) either have symptoms of or have been diagnosed with “POTS” or “dysautonomia” It is estimated that up to 70% of HSD hEDS patients report symptoms consistent with dysautonomia and up to 40% meet diagnostic criteria for POTS The purpose of this post is to provide a brief overview of the answers to the
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