Ehlers-Danlos syndrome (Q46617): Difference between revisions
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A síndrome de Ehlers-Danlos (SED) é um grupo heterogêneo de doenças hereditárias do tecido conjuntivo, principalmente do colágeno, que variam em gravidade, desde hipermobilidade articular leve até fragilidade de tecidos moles e vasos sanguíneos com risco de vida. | |||
| description / en | description / en | ||
Ehlers-Danlos syndrome (EDS) is a heterogeneous group of inherited disorders of connective tissue, principally collagen, that range in severity from mild joint hypermobility to life-threatening fragility of soft tissue and vasculature. | |||
Revision as of 15:19, 13 August 2026
Ehlers-Danlos syndrome (EDS) is a heterogeneous group of inherited disorders of connective tissue, principally collagen, that range in severity from mild joint hypermobility to life-threatening fragility of soft tissue and vasculature.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LD28.1 |
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| English | Ehlers-Danlos syndrome |
Ehlers-Danlos syndrome (EDS) is a heterogeneous group of inherited disorders of connective tissue, principally collagen, that range in severity from mild joint hypermobility to life-threatening fragility of soft tissue and vasculature. |
