Síndrome de Ehlers-Danlos con especial énfasis en el síndrome de hiperlaxitud articular: [revisión] / Ehlers-Danlos syndrome, with special emphasis in the joint hypermobility syndrome: [review]
Rev. méd. Chile
;
137(11): 1488-1497, nov. 2009. tab, ilus
Article
in Spanish
| LILACS
| ID: lil-537014
ABSTRACT
There 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.
Full text:
Available
Index:
LILACS (Americas)
Main subject:
Ehlers-Danlos Syndrome
/
Joint Instability
Type of study:
Diagnostic study
Limits:
Adolescent
/
Humans
Language:
Spanish
Journal:
Rev. méd. Chile
Journal subject:
Medicine
Year:
2009
Type:
Article
Affiliation country:
Chile
Institution/Affiliation country:
Universidad de Chile/CL
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