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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Translation of “Hiperlaxitud articular” in English
April – June Pages The main hiperepasticidad diagnosis is other types of EDS, particularly those characterized by significant connective tissue abnormalities.
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. Check this box if you wish to receive a copy of your message.
For all other comments, please send your remarks via contact us. Complications often include chronic pain affecting physical activity, fatigue, sleep disorders, early osteoarthritis and osteoporosis, and cardiovascular symptoms chest pain, palpitations, postural instability.
Orphanet: S ndrome de hiperlaxitud articular benigno
Most affected patients are female. Enfoques top-down y bottom-up para el tratamiento de la 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 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. Perucho Pont a. 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.
Some cases may be autosomal recessive. You can change the settings or obtain more information by clicking here. Print Send to a friend Export reference Mendeley Statistics. Diagnosis is currently based on major and minor diagnostic criteria including clinical signs and family history as defined in the Villefranche classification.
Hiperlaxitud Articular | O_O | Guillermo Salinas | Flickr
Management and treatment There is no specific treatment. It is not known whether penetrance is complete but there is highly variable expressivity. SRJ is a prestige metric based on the idea that not all citations are the hipedelasticidad.
Si continua navegando, consideramos que acepta su uso. The primary manifestation is hyperlaxity involving any joints: Only comments written in English can be processed.
It does not have a specific treatment. The documents contained in this web site are presented for information purposes only. Professionals Summary information Greekpdf Suomipdf Russianpdf Anesthesia guidelines Englishpdf Deutschpdf Guidance for genetic testing Englishpdf Clinical genetics review English Specialised Social Services Eurordis directory.
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Wide clinical variability is found. De novo events should be suspected if the parents of an affected patient have no signs of EDS.
Patients may also have soft or mildly hyperextensible skin, easy bruising and bleeding disorders. 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.
Additional information Further information on this disease Classification s 4 Gene s 1 Clinical signs and symptoms Publications in PubMed Other website s 8. Genetic counseling Transmission is autosomal dominant. 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. Previous article Next article.