Síndrome de Ehlers-Danlos con especial énfasis en el síndrome de hiperlaxitud articular

dc.creatorBravo,Jaime F
dc.date2009-11-01
dc.date.accessioned2017-03-07T16:17:56Z
dc.date.available2017-03-07T16:17:56Z
dc.identifierhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872009001100013
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/399233
dc.descriptionThere is an urgent need to increase the awareness on the Joint Hyper mobility Syndrome QHS). This is a congenital and prevalent emergent condition that is frequently undiagnosed and that causes significant health problems. Besides recurrent muscular-skeletal problems and signs and symptoms derived from tissue fragility, adolescents and young adults may develop osteoporosis, early osteoarthritis or dysautonomia, that are common in the disease, and deteriorate quality of life. Many JHS patients have signs and symptoms suggestive of fibromyalgia and are usually misdiagnosed. Physicians should be able to differentiate the less severe form of JHS from the Vascular Ehlers-Danlos Syndrome, to diagnose it before the appearance of serious complications and even death. The study of these diseases is a promising area for genomic and rheumatologic research.
dc.formattext/html
dc.languagees
dc.publisherSociedad Médica de Santiago
dc.sourceRevista médica de Chile v.137 n.11 2009
dc.subjectEhlers-Danlos syndrome
dc.subjectFibromyalgia
dc.subjectJoint instability
dc.titleSíndrome de Ehlers-Danlos con especial énfasis en el síndrome de hiperlaxitud articular
dc.typeArtículos de revistas


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