The Ehlers Danlos syndrome : a rare disease although commonly suspected
The Ehlers Danlos syndromes (EDS) are a heterogenous group of inherited connective tissue disorders characterized by generalized joint hypermobility and instability, tissue fragility and multiple functional disorders. The EDS hypermobility type (hEDS) is the most common but the mildest subtype of EDS and is defined by joint involvement. hSED diagnosis is based on clinical criteria because no genetic factors nor molecular basis have yet been identified. Since chronic pain constitutes one of hESD main symptoms, the diagnosis is frequently suspected although the syndrome is rare, with a prevalence estimated to be 1/10.000. An expert clinical evaluation is therefore necessary in order to establish an accurate diagnosis. This allows the implementation of physical therapy which is the only treatment that has proven efficacious in reducing joint instability, generalized pain and secondary osteoarthritis.
| Medienart: |
Artikel |
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| Erscheinungsjahr: |
2023 |
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| Erschienen: |
2023 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:78 |
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| Enthalten in: |
Revue medicale de Liege - 78(2023), 11 vom: 13. Nov., Seite 626-633 |
| Sprache: |
Französisch |
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| Weiterer Titel: |
Le syndrome d’Ehlers Danlos : une maladie rare fréquemment suspectée |
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| Beteiligte Personen: |
Docampo, Elisa [VerfasserIn] |
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| Themen: |
Chronic pain |
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| Anmerkungen: |
Date Completed 14.11.2023 Date Revised 14.11.2023 published: Print Citation Status MEDLINE |
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| Förderinstitution / Projekttitel: |
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NLM364469463 |
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| 520 | |a The Ehlers Danlos syndromes (EDS) are a heterogenous group of inherited connective tissue disorders characterized by generalized joint hypermobility and instability, tissue fragility and multiple functional disorders. The EDS hypermobility type (hEDS) is the most common but the mildest subtype of EDS and is defined by joint involvement. hSED diagnosis is based on clinical criteria because no genetic factors nor molecular basis have yet been identified. Since chronic pain constitutes one of hESD main symptoms, the diagnosis is frequently suspected although the syndrome is rare, with a prevalence estimated to be 1/10.000. An expert clinical evaluation is therefore necessary in order to establish an accurate diagnosis. This allows the implementation of physical therapy which is the only treatment that has proven efficacious in reducing joint instability, generalized pain and secondary osteoarthritis | ||
| 650 | 4 | |a English Abstract | |
| 650 | 4 | |a Journal Article | |
| 650 | 4 | |a Chronic pain | |
| 650 | 4 | |a Clinical criteria | |
| 650 | 4 | |a Ehlers Danlos | |
| 650 | 4 | |a Joint hypermobility | |
| 650 | 4 | |a Physical therapy | |
| 700 | 1 | |a Lehane, Florence |e verfasserin |4 aut | |
| 700 | 1 | |a Ribbens, Clio |e verfasserin |4 aut | |
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