Translations in context of “Hiperlaxitud articular” in Spanish-English from Reverso Context: Leve curvatura espinal Hiperlaxitud articular deficiencia de los . También presentan hiperlaxitud articular, a veces con subluxaciones recurrentes , piel extensible y friable, con moretones fáciles y alteración ocular, con. El síndrome de hiperlaxitud articular (SHA) se caracteriza por la presencia de hiperlaxitud articular y síntomas en relación con el aparato locomotor. La etiología.

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Enfoques top-down y bottom-up para el tratamiento de la Most affected patients are female. The most frequent symptom is the musculo-skeletal pain. You can change the settings or obtain more information by clicking here.

Specialised Social Services Eurordis directory. Wide clinical variability is found. The underlying pathogenic mechanism is unknown. Other search option s Alphabetical list.

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

Other diseases that also involve joint laxity are generally easy to distinguished from EDS by their characteristic features. Surgical procedures should be hiperelasticifad with caution. It does not have a specific treatment. Etiology The underlying pathogenic mechanism is unknown.

Síndrome de hiperlaxitud articular. A propósito de un caso | Rehabilitación

Gastrointestinal involvement with functional bowel disorders is common, while esophageal hypomobility, gastroesophageal reflux and gastritis are sometimes found. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field.


Diagnosis is currently based on major and minor diagnostic criteria including clinical signs and family history as defined hiperellasticidad the Villefranche classification. SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact. Additional information Further information on this disease Classification s 4 Gene s 1 Clinical signs and symptoms Publications in PubMed Other website s 8. 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.

Supportive and symptomatic individualized treatments include physical therapy, rehabilitation, assistive devices, pain medications, and suitable therapy for extra-articular manifestations. April – June Pages Hyperlaxity is more pronounced in younger patients and in females.

A small number of patients have been found to have haploinsufficiency of tenascin X, a glycoprotein hiperelastiicdad in connective tissues and encoded by the TNXB gene 6p Patients may also have soft or mildly hyperextensible skin, easy bruising and bleeding disorders.

Differential diagnosis The main differential diagnosis is other types of EDS, particularly those characterized by significant connective tissue abnormalities.

Hiperlaxitud Articular

To improve our services and products, we use hiperdlasticidad own or third parties authorized to hiperelasticodad advertising related to client preferences through the analyses of navigation customer behavior. 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. 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.


There is still debate as to whether benign joint hypermobility syndrome BJHS is a distinct disorder or part of a clinical continuum. There is no increased risk of early mortality but high morbidity due to joint hyperlaxity, chronic and hiperleasticidad pain as well as extra-musculoskeletal manifestations which all greatly diminish quality of life.

Subscribe to our Newsletter. The most frequent symptom is the musculo-skeletal pain. Si hiperelasticidd navegando, consideramos que acepta su uso. Supportive diagnostic criteria include a positive family history, recurrent joint instability, and easy bruising.

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Antenatal diagnosis Prenatal testing is not available articilar the absence of an identified causal gene mutation. Only comments written in English can be processed. The most frequent symptom is the musculoskeletal pain.