Respiratory surveillance of patients with Duchenne and Becker muscular dystrophy.


Autoria(s): Spehrs-Ciaffi V.; Fitting J.W.; Cotting J.; Jeannet P.Y.
Data(s)

2009

Resumo

Duchenne muscular dystrophy is is the most common form of the childhood muscular dystrophies. It follows a predictable clinical course marked by progressive skeletal muscle weakness, lost of ambulation before teen-age and death in early adulthood secondary to respiratory or cardiac failure. Becker muscular dystrophy is less common and has a milder clinical course but also results in respiratory and cardiac failure.Altough recent advances in respiratory care and new technologies have improved the outlook many patients already received only a traditional non-interventional approach. The aims of this work are: to analyse the pathophysiology and natural history of respiratory function in these diseases, to descript their clinical manifestations, to present the diagnostics tools and to provide recommendations for an adequated respiratory care in this particular population based on the updated literature referenced.

Identificador

http://serval.unil.ch/?id=serval:BIB_5C20BDBDD61F

isbn:1874-5393 (Print)

pmid:21791803

doi:10.3233/PRM-2009-0071

Idioma(s)

en

Direitos

info:eu-repo/semantics/openAccess

Fonte

Journal of Pediatric Rehabilitation Medicine, vol. 2, no. 2, pp. 115-122

Tipo

info:eu-repo/semantics/article

article