Se seleccionaron pacientes con diagnóstico de hiperelasticidad cutánea o hiperlaxitud articular; se realizó la historia clínica y exploración. Request PDF on ResearchGate | On Jan 1, , Carolina Baeza-Velasco and others published Sintomatología ansiosa y síndrome de hiperlaxitud articular en . El Síndrome de Ehlers-Danlos tipo III (SED-III), tam- bién llamado Síndrome de Hiperlaxitud Articular (SHA), es una enfermedad de los tejidos conectivos, muy.

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Diagnostic methods Diagnosis is currently based on major and minor diagnostic criteria including clinical signs and family history as defined in the Villefranche classification. The documents contained in this web site are presented for information purposes only.

Annals of the Rheumatic Diseases. Major diagnostic criteria include joint hyperlaxity, soft skin or skin hyperextensibility, and an absence of other significant skin or soft tissue fragility.

Complications often include chronic pain affecting physical activity, fatigue, sleep disorders, early hiperlaxitus and osteoporosis, and cardiovascular symptoms chest pain, palpitations, postural instability. Genetic counseling Transmission is autosomal dominant. Se toma en consideraciones los siguientes indicadores: The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.

Patients may also have soft or mildly hyperextensible skin, easy bruising and bleeding disorders. From Monday to Friday from 9 a. Se atiende hiperlaxitus tipo de deformidad asociada Columna, Rodilla y Pie.


The most frequent symptom is the musculo-skeletal pain.

There is still debate as to whether benign joint hypermobility syndrome BJHS is a distinct disorder or part of a clinical continuum. De novo events should be suspected if the parents of an affected patient have no signs of EDS. Disease definition 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.

Si EEP es mayor que 8, la estrategia se considera fuerte. The hypermobility syndrome is characterized by the presence of joint hyperlaxity and musculoskeletal symptoms. Joint hypermobility and genetic collagen disorders are they related. The main differential diagnosis is other types of EDS, particularly those characterized by significant connective tissue abnormalities. Supportive diagnostic criteria include a positive family history, recurrent joint instability, and easy bruising.

Management and treatment There is no specific treatment. Mejorar la fuerza muscular y tono muscular. To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior.

Hiperlaxitud Articular

Continuing navigation will be considered as acceptance of this use. CiteScore measures average citations received per document published. A small number of patients have been found to have haploinsufficiency of tenascin X, a glycoprotein expressed in connective tissues and encoded by the TNXB gene 6p For this reason a program of physical-therapeutic exercises was designed to contribute to the relief of bone muscle articulate System ailments so that the affected ones can have a greater participation in the different school activities and of the daily life.


The most frequent symptom is the musculo-skeletal pain.

Orphanet: S ndrome de hiperlaxitud articular benigno

Mejorar los niveles de resistencia y resistencia a la fuerza muscular. The hypermobility syndrome is characterized by the presence of joint hyperlaxity and musculoskeletal symptoms. Rev Cubana de Reumatol.

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Conclusions and recommendations were reached. This was judged by specialists. The specialists considered the implementation of the program with a Strong Expected Effectiveness very appropriate.

Hiperlaxitud Articular | Joint hypermobility. | Joint Hypermobility Syndrome | Flickr

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. Prognosis There is no increased risk of early mortality but high morbidity due to joint hyperlaxity, chronic and acute pain as well as extra-musculoskeletal manifestations which all greatly diminish quality of life.

We analyzed the theoretical and methodological foundations of hiperlaxifud rehabilitation treatment in adolescents to establish the diagnosis of the treatment. It does not have a specific treatment.