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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Hiperlaxitud Articular

Onset can be at any age but hiperrelasticidad is difficult to assess in young children due to higher joint laxity at this age. Additional information Further information on this disease Classification s 4 Gene s 1 Clinical signs and symptoms Publications in PubMed Other website s 8.

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Translation of “Hiperlaxitud articular” in English

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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.

Other search option s Alphabetical list. De novo events should be suspected if the parents of an affected patient have no signs of EDS.

Its etiology is not absolutely well-known. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field. Health care resources for this disease Expert centres Diagnostic tests 35 Patient organisations 42 Orphan drug s 0.

These figures may however be underestimated due to clinical variability. Etiology The underlying pathogenic mechanism is unknown.

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 hiperelaaticidad of life. 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 The underlying pathogenic mechanism is unknown.

síndrome de ehlers-danlos y síndrome de hiperlaxitud articular – | EDS | Pinterest

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Supportive diagnostic criteria include a positive family history, recurrent joint instability, and easy bruising. The hypermobility syndrome is characterized by the presence of joint hyperlaxity and musculoskeletal symptoms.


Transmission is autosomal dominant. For all other comments, please send your remarks via contact us. Management and treatment There is no specific treatment.

Hiperlaxitud articular – Translation into English – examples Spanish | Reverso Context

The hypermobility syndrome is characterized by the presence of joint hyperlaxity and musculoskeletal symptoms. Some cases may be autosomal recessive. The most frequent symptom is the musculoskeletal pain. You can change the settings or obtain more information by clicking here.

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. April – June Pages It does not have a specific treatment. The primary manifestation is hyperlaxity involving any joints: The currently available scoring criteria Beighton score have been demonstrated to be highly variable among investigators.