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Aran-Duchenne disease
Cruveilhier disease
Degeneration of iris
Distal
Fazio-Londe
Infantile spinal muscular atrophy
Kugelberg-Welander
PMA
Primary
Progressive bulbar palsy
Progressive bulbar palsy of childhood
Progressive cerebellar atrophy
Progressive muscular atrophy
Progressive muscular atrophy of infancy
Progressive spinal muscular atrophy
Pupillary margin
SMA
SMA I
SPMA
Scapuloperoneal form
Severe infantile spinal muscular atrophy
Spinal muscular atrophy
Spinal muscular atrophy adult form
Spinal muscular atrophy type I
Spinal progressive muscular atrophy
Werdnig-Hoffman disease

Vertaling van "Progressive cerebellar atrophy " (Engels → Nederlands) :

progressive cerebellar atrophy
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
progressieve cerebellumatrofie
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Aran-Duchenne disease | Cruveilhier disease | PMA | progressive muscular atrophy | progressive spinal muscular atrophy | spinal muscular atrophy | spinal progressive muscular atrophy | SMA [Abbr.] | SPMA [Abbr.]
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
spieratrofie van Aran-Duchenne | ziekte van Duchenne-Aran
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
A rare genetic neurological disorder characterized by late childhood onset of slowly progressive cerebellar ataxia. Initial manifestations include weakness and atrophy of distal limb muscles, areflexia and loss of pain, vibration and touch sensations
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
spinocerebellaire ataxie met axonale neuropathie type 1
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
A rare mitochondrial oxidative phosphorylation disorder due to nuclear deoxyribonucleic acid anomalies. The disease is characterised by progressive external ophthalmoplegia without diplopia, cerebellar atrophy, proximal skeletal muscle weakness with
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
progressieve externe oftalmoplegie, myopathie, emaciatie
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
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.]
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
infantiele spinale spieratrofie | Spinale musculaire atrofie type I | ziekte van Werdnig-Hoffmann | SMA type I [Abbr.]
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Spinocerebellar ataxia type 28 (SCA28) is very rare with main features of juvenile onset and slowly progressive cerebellar ataxia due to Purkinje cell degeneration. The mean age of symptom onset was 19.5 years in the original kindred. Some patients s
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
spinocerebellaire ataxie type 28
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
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
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
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
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
Degeneration of:iris (pigmentary) | pupillary margin | Iridoschisis Iris atrophy (essential)(progressive) Miotic pupillary cyst Translucency of iris
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
degeneratie van | iris (pigmentair) | degeneratie van | pupilrand | iridoschisis | irisatrofie (essentieel)(progressief) | miotische pupilcyste | lichtdoorlatende iris
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
Familial motor neuron disease Lateral sclerosis:amyotrophic | primary | Progressive:bulbar palsy | spinal muscular atrophy
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
familiale ziekte van motorische neuronen | laterale sclerose | amyotrofe | laterale sclerose | primaire | progressieve | bulbairparalyse | progressieve | spinale spieratrofie
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]


Anderen hebben gezocht naar : aran-duchenne disease     cruveilhier disease     degeneration of iris     fazio-londe     kugelberg-welander     progressive bulbar palsy of childhood     progressive bulbar palsy     spinal muscular atrophy adult form     werdnig-hoffman disease     childhood form type ii     distal     infantile spinal muscular atrophy     juvenile form type iii     primary     progressive cerebellar atrophy     progressive muscular atrophy     progressive muscular atrophy of infancy     progressive spinal muscular atrophy     pupillary margin     scapuloperoneal form     severe infantile spinal muscular atrophy     spinal muscular atrophy     spinal muscular atrophy type     spinal progressive muscular atrophy     Progressive cerebellar atrophy     


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'Progressive cerebellar atrophy' ->

Date index: 2022-07-12
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