Vertaling van "diafragmatische spinale spieratrofie type " (Nederlands → Engels) :

diafragmatische spinale spieratrofie type 2
Diaphragmatic spinal muscular atrophy type 2

progressieve bulbairparalyse in kinderjaren [Fazio-Londe] | spinale spieratrofie | distaal | spinale spieratrofie | juveniele vorm, type III [Kugelberg-Welander] | spinale spieratrofie | scapuloperoneale vorm | spinale spieratrofie | van kinderleeftijd, type II | spinale spieratrofie | volwassen vorm
Progressive bulbar palsy of childhood [Fazio-Londe] Spinal muscular atrophy:adult form | childhood form, type II | distal | juvenile form, type III [Kugelberg-Welander] | scapuloperoneal form

infantiele spinale spieratrofie | Spinale musculaire atrofie type I | ziekte van Werdnig-Hoffmann | SMA type I [Abbr.]
infantile spinal muscular atrophy | progressive muscular atrophy of infancy | severe infantile spinal muscular atrophy | spinal muscular atrophy type I | Werdnig-Hoffman disease | SMA I [Abbr.]

spinale musculaire atrofie type III | spinale spieratrofie type III | ziekte van Kugelberg-Welander | ziekte van Wohlfart-Kugelberg-Welander | SMA III [Abbr.]
juvenile spinal muscular atrophy | Kugelberg-Welander disease | spinal muscular atrophy type III | Wohlfart-Kugelberg-Welander disease | SMA III [Abbr.]

spinale spieratrofie met respiratoire insufficiëntie type 1
Distal spinal muscular atrophy type 1

spinale spieratrofie met respiratoire insufficiëntie type 2
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

infantiele spinale-spieratrofie, type I [Werdnig-Hoffman]
Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]