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Becker
Benign
Benign scapuloperoneal with early contractures
Congenital muscular dystrophy NOS
DMD
Disease central core
Distal
Duchenne
Duchenne muscular dystrophy
Duchenne type muscular dystrophy
Duchenne's muscular dystrophy
Eichhorst type
Emery-Dreifuss
Facioscapulohumeral
Limb-girdle
MD
Meryon's disease
Minicore
Multicore
Muscular dystrophy
Muscular dystrophy - Duchenne type
Nemaline
Ocular
Oculopharyngeal
Progressive muscular dystrophy
Progressive muscular dystrophy Eichhorst
Pseudohypertrophic muscular dystrophy
Scapulohumeral muscular dystrophy
Scapuloperoneal
Severe

Traduction de «Scapulohumeral muscular dystrophy » (Anglais → Néerlandais) :

Scapulohumeral muscular dystrophy

scapulohumerale dystrofie


Duchenne muscular dystrophy | Duchenne type muscular dystrophy | Duchenne's muscular dystrophy | Meryon's disease | Muscular dystrophy - Duchenne type | pseudohypertrophic muscular dystrophy | DMD [Abbr.]

Duchenne spierdystrofie | pseudohypertrofische musculaire dystrofie


Eichhorst type | progressive muscular dystrophy | progressive muscular dystrophy Eichhorst

type van Eichhorst




A rare progressive muscular dystrophy characterized by an adult-onset scapulo-axio-peroneal myopathy. Clinical presentation includes shoulder girdle atrophy, scapular winging, axial muscular atrophy of postural muscles combined with a generalized hyp

X-gebonden myopathie met posturale spieratrofie


Muscular dystrophy:autosomal recessive, childhood type, resembling Duchenne or Becker | benign [Becker] | benign scapuloperoneal with early contractures [Emery-Dreifuss] | distal | facioscapulohumeral | limb-girdle | ocular | oculopharyngeal | scapuloperoneal | severe [Duchenne]

spierdystrofie | autosomaal recessief, op kinderleeftijd, gelijkend op Duchenne of Becker | spierdystrofie | benigne [Becker] | spierdystrofie | benigne scapuloperoneaal met vroege contracturen [Emery-Dreifuss] | spierdystrofie | distaal | spierdystrofie | ernstig [Duchenne] | spierdystrofie | facioscapulohumeraal | spierdystrofie | schouder- en bekkengordel | spierdystrofie | oculair | spierdystrofie | oculofaryngeaal | spierdystrofie | scapuloperoneaal


Autosomal dominant limb girdle muscular dystrophy type 1A

autosomaal dominante limb-girdle-spierdystrofie type 1A


Congenital muscular dystrophy:NOS | with specific morphological abnormalities of the muscle fibre | Disease:central core | minicore | multicore | Fibre-type disproportion Myopathy:myotubular (centronuclear) | nemaline

central-core-disease | congenitale spierdystrofie | NNO | congenitale spierdystrofie | met specifieke morfologische-afwijkingen van spiervezel | fibre-type disproportion | minicore disease | multicore disease | myopathie | myotubulair (centronucleair) | myopathie | nemaline lichaampjes




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