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Kies diagnose... Duchenne spierdystrofie
Alle diagnoses amyotrofische laterale sclerose arthrogryposis multiplex congenita ataxie van Friedreich Autoimmuun myositis, overige Autosomale recessieve Duchenne spierdystrofie Barth syndroom Becker myotonie Becker spierdystrofie Bethlem, ziekte van carnitinedeficiëntie central core disease centronucleaire myopathie chronische idiopathische axonale polyneuropathie chronische inflammatoire demyeliniserende polyneuropathie congenitale myasthenia gravis congenitale myopathie met cytoplasmic bodies Congenitale myopathieën n.n.b. congenitale myotonie congenitale spierdystrofie congenitale vezel type disproportie dermatomyositis distale spinale spieratrofieën Duchenne spierdystrofie Dunnevezel-neuropathie dystrofieën Emery-Dreifuss spierdystrofie erfelijke drukneuropathie Eulenberg myotonie facioscapulohumerale dystrofie focale spinale spieratrofieën Fukuyama congenitale spierdystrofie glycogenose III glycogenose IV glycogenose V glycogenose VII Guillain-Barré syndroom hereditaire motorische en sensorische neuropathie n.n.b. hereditaire motorische sensorische neuropathie type 1 hereditaire motorische sensorische neuropathie type 2 hereditaire motorische sensorische neuropathie type 3 hereditaire motorische sensorische neuropathie type 4 hereditaire motorische sensorische neuropathie type 5 hereditaire motorische sensorische neuropathie X-gebonden hereditaire neuralgische amyotrofie hereditaire sensorische autonome neuropathie Hereditaire Spastische Paraparese idiopatische neuralgische amyotrofie inclusion body myositis Kearns-Sayre syndroom Kennedy, ziekte van Laing distale myopathie Lambert-Eaton myastheen syndroom laterale sclerose Leyden-Erb spierdystrofie limb-girdle spierdystrofie macrofage myofasciitis Markesbery-Griggs distale myopathie metabole myopathieën Miller-Fisher syndroom minicore of multicore myopathie mitochondriële myopathieën Miyoshi distale myopathie monoclonal gammopathy of undetermined significance polyneuropathie multifocale motore neuropathie myastenieën n.n.b. myastheen syndroom myasthenia gravis myopathieën myositis n.n.b. myositis ossificans progressiva myotone dystrofie myotonieën n.n.b. myotubulaire myopathie nemaline myopathie Neuralgische amyotrofie Nonaka distale myopathie oculaire myopathie oculopharyngeale spierdystrofie opthalmoplegie overige groepen spierziekten periodieke erfelijke verlammingsziekten periodieke niet-erfelijke verlammingsziekten Periodieke verlammingsziekten Poland, syndroom van polio en postpolio-syndroom polymyositis polyneuropathie Pompe, Ziekte van potassium-aggrevated myotonias progressieve spinale musculaire atrofie proximale myotone myopathie rhabdomyelise rigid spine syndroom scapuloperoneaal syndroom spierdystrofieën en distale myopathieën n.n.b. Spinale spieratrofieën n.n.b. spinale spieratrofieën type 1 spinale spieratrofieën type 2 spinale spieratrofieën type 3 Thomsen myotonie Welander distale myopathie
 
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Artikel detail
0000 - A Dutch Guideline for the Treatment of Neuromuscular Scoliosis

Artikel omschrijving:

ABSTRACT
Children with neuromuscular disorders with a progressive muscle weakness such as Duchenne Muscular Dystrophy and Spinal Muscular Atrophy frequently develop a progressive scoliosis. A severe scoliosis compromises respiratory function, makes sitting more difficult, and is perceived as unaesthetic. Spinal surgery is considered the primary treatment option for correcting severe neuromuscular scoliosis. Surgery in this population requires a multidisciplinary approach, careful planning, dedicated surgical procedures, and specialized aftercare. In order to optimize the treatment for neuromuscular scoliosis a Dutch guideline has been composed addressing conservative treatment, the preoperative, perioperative, and postoperative care of neuromuscular scoliosis. The guideline is based on scientific evidence and expert opinions. For most aspects of the treatment scientific evidence is scarce and only low level cohort studies were found. Nevertheless, a high degree of consensus was reached about the management of patients with neuromuscular scoliosis. This was translated into a set of recommendations, which are now accepted as a general guideline in the Netherlands.

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http://www.scoliosisjournal.com/content/3/1/14

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