Vertaling van "benign scapuloperoneal with early contractures " (Engels → Nederlands) :

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

A rare distal hereditary motor neuropathy with a variable clinical phenotype and typical characteristics of congenital, non-progressive, predominantly distal lower limb muscle weakness and atrophy and congenital (or early-onset) flexion contractures
autosomaal dominante congenitale benigne spinale spieratrofie

A central nervous system malformation with characteristics of severe intellectual deficit, early hypotonia with progression to spasticity and contractures, choreoathetosis, seizures, dysmorphic face (long face with prominent forehead) and brain imagi
X-gebonden intellectuele achterstand, malformatie van Dandy-Walker, basale gangliaziekte, insultensyndroom

A rare genetic motor neuron disease with characteristics of progressive early respiratory failure associated with diaphragm paralysis, distal muscular weakness, joint contractures, and axial hypotonia with preserved antigravity limb movements. The ph
spinale spieratrofie met respiratoire insufficiëntie type 2