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Amyotrophie d'Aran-Duchenne
Amyotrophie primitive progressive
Amyotrophie progressive
Amyotrophie spinale progressive
Ataxie cérébelleuse liée à l'X non progressive
Atrophie cérébelleuse
Atrophie cérébelleuse progressive
Atrophie de Cruveilhier
Atrophie hémifaciale progressive
Atrophie musculaire progressive
Atrophie musculaire progressive d'Aran
Dystrophie musculaire progressive
Maladie d'Aran-Duchenne
Myopathie atrophique progressive
Myopathie primitive progressive
Rebord pupillaire

Translation of "atrophie cérébelleuse progressive " (French → English) :

atrophie cérébelleuse progressive

progressive cerebellar atrophy
IATE - Health
IATE - Health


myopathie primitive progressive | dystrophie musculaire progressive | myopathie atrophique progressive | amyotrophie primitive progressive | amyotrophie progressive | atrophie musculaire progressive

progressive muscular dystrophy | Erb-Landouzy disease | Erb's disease | idiopathic muscular atrophy | myodystrophia
médecine
médecine


amyotrophie d'Aran-Duchenne | amyotrophie spinale progressive | atrophie de Cruveilhier | atrophie musculaire progressive d'Aran | maladie d'Aran-Duchenne

Aran-Duchenne disease | Cruveilhier disease | PMA | progressive muscular atrophy | progressive spinal muscular atrophy | spinal muscular atrophy | spinal progressive muscular atrophy | SMA [Abbr.] | SPMA [Abbr.]
IATE - Health
IATE - Health


atrophie cérébelleuse

alcoholic cerebellar degeneration
Système nerveux
Nervous System


atrophie de Cruveilhier | atrophie musculaire progressive

Cruveilhier atrophy
IATE - Health
IATE - Health


atrophie musculaire progressive

progressive spinal muscular atrophy
Système nerveux
Nervous System


atrophie musculaire progressive

Duchenne-Aran muscular atrophy
SNOMEDCT-BE (disorder) / 88923002
SNOMEDCT-BE (disorder) / 88923002


atrophie hémifaciale progressive

Romberg syndrome
SNOMEDCT-BE (disorder) / 718224004
SNOMEDCT-BE (disorder) / 718224004


ataxie cérébelleuse liée à l'X non progressive

A rare hereditary ataxia with characteristics of delayed early motor development, severe neonatal hypotonia, non-progressive ataxia and slow eye movements, presenting normal cognitive abilities and absence of pyramidal signs. Frequently patients also
SNOMEDCT-BE (disorder) / 766818009
SNOMEDCT-BE (disorder) / 766818009


Atrophie de l'iris (essentielle) (progressive) Dégénérescence de:iris (pigmentaire) | rebord pupillaire | Iridoschisis Kyste pupillaire miotique Translucidité de l'iris

Degeneration of:iris (pigmentary) | pupillary margin | Iridoschisis Iris atrophy (essential)(progressive) Miotic pupillary cyst Translucency of iris
WORLD HEALTH ORGANIZATION ICD-10: H21.2
WORLD HEALTH ORGANIZATION ICD-10: H21.2




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atrophie cérébelleuse progressive

Date index:2023-11-23 -

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