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Meztijas Management and treatment There is no specific treatment. Hiperlaxitud Articular Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted.
The most frequent symptom is the musculo-skeletal pain. Transmission is autosomal dominant. These figures may however be underestimated due to clinical variability.
Hyperlaxity is more pronounced in younger patients and in females. Ehlers-Danlos syndrome, hypermobility type HT-EDS is the most frequent form of EDS see this terma group of hereditary connective tissue diseases, and is characterized by joint hyperlaxity, mild skin hyperextensibility, tissue fragility and extra-musculoskeletal manifestations.
Professionals Summary information Greekpdf Suomipdf Russianpdf Anesthesia guidelines Englishpdf Deutschpdf Guidance for genetic testing Englishpdf Clinical genetics review English Clinical description Onset can be at any age but it is difficult to assess in young children due to higher joint laxity at this age.
Diagnosis is currently based on major and minor diagnostic criteria including clinical signs and family history as defined in the Villefranche classification.
The underlying pathogenic mechanism is unknown. It is important to take preventive measures, to do a symptomatic treatment and an individualized physical preparation program under the supervision of a rehabilitation medicine specialist.
Antenatal diagnosis Prenatal testing is not available in the absence of an identified causal gene mutation. Print Send to a friend Export reference Mendeley Statistics. It is important to take preventive measures to do a symptomatic treatment and an individualized physical preparation program under the supervision of a rehabilitation medicine specialist. The hypermobility syndrome is characterized by the presence of joint hyperlaxity and musculoskeletal symptoms.
Differential diagnosis The main differential diagnosis is other types of EDS, particularly those characterized by significant connective tissue abnormalities. Some cases may be autosomal recessive. Complications often include hperelasticidad pain affecting physical activity, fatigue, sleep disorders, early osteoarthritis and osteoporosis, and cardiovascular symptoms chest pain, palpitations, postural instability.
Major diagnostic criteria include joint hyperlaxity, soft skin or skin hyperextensibility, and an absence of other significant skin or soft tissue fragility. Onset can be at any age but it is difficult to assess in young children due to higher joint laxity at this age. CiteScore measures average citations received per document published. The main differential diagnosis is other types of EDS, particularly those characterized by significant connective tissue abnormalities.
The diagnosis of this syndrome is clinical. Surgical procedures should be considered with caution. Previous article Next article. It does not have a specific treatment. For all other comments, please send your remarks via contact us. Health care resources for this disease Expert centres Diagnostic tests 35 Patient organisations 42 Orphan drug s 0.
Supportive diagnostic criteria include a positive family history, recurrent joint instability, and easy bruising. Gastrointestinal involvement with functional bowel disorders is common, while esophageal hypomobility, gastroesophageal reflux and gastritis are sometimes found. Related Articles
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Meztijas Management and treatment There is no specific treatment. Hiperlaxitud Articular Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. The most frequent symptom is the musculo-skeletal pain. Transmission is autosomal dominant. These figures may however be underestimated due to clinical variability.
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