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Ehlers–Danlos syndromes (EDS) are a group of 13 genetic connective tissue disorders. Symptoms often include loose joints, joint pain, stretchy, velvety skin, and abnormal scar formation. These may be noticed at birth or in early childhood. Complications may include aortic dissection, joint dislocations, scoliosis, chronic pain, or early osteoarthritis.…
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| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Ehlers–Danlos syndrome | Causes | Genetic | 1.00 | infobox |
| Ehlers–Danlos syndrome | Complications | Aortic dissection, joint dislocations, osteoarthritis, amplified musculoskeletal pain syndrome | 1.00 | infobox |
| Ehlers–Danlos syndrome | Diagnostic method | Genetic testing, physical examination | 1.00 | infobox |
| Ehlers–Danlos syndrome | Differential diagnosis | Marfan syndrome, cutis laxa syndrome, familial joint hypermobility syndrome, Loeys–Dietz syndrome, hypermobility spectrum disorder | 1.00 | infobox |
| Ehlers–Danlos syndrome | Duration | Lifelong | 1.00 | infobox |
| Ehlers–Danlos syndrome | Frequency | 1 in 5,000 overall, 7.5 in 1,000 to 20 in 1,000 for hEDS | 1.00 | infobox |
| Ehlers–Danlos syndrome | Prognosis | Depends on specific disorder | 1.00 | infobox |
| Ehlers–Danlos syndrome | Pronunciation | /ˈeɪlərz ˈdænlɒs/ | 1.00 | infobox |
| Ehlers–Danlos syndrome | Risk factors | Family history | 1.00 | infobox |
| Ehlers–Danlos syndrome | Specialty | Medical genetics | 1.00 | infobox |
| Ehlers–Danlos syndrome | Symptoms | Overly flexible joints, stretchy skin, abnormal scar formation | 1.00 | infobox |
| Ehlers–Danlos syndrome | Treatment | Supportive | 1.00 | infobox |
| Ehlers–Danlos syndrome | Types | Hypermobile, classic, vascular, kyphoscoliosis, arthrochalasia, dermatosparaxis, brittle cornea syndrome, others | 1.00 | infobox |
| Ehlers–Danlos syndrome | Usual onset | Childhood or adolescence, depending on type | 1.00 | infobox |
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