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

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ataxie spinocérébelleuse type 28

SNOMEDCT-BE (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 / 715824008

SNOMEDCT-BE (disorder) / 715824008

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A rare endocrine disease with characteristics of the triad of adult-onset diabetes mellitus, progressive hearing loss (usually presenting in the first decade of life and principally of low to moderate frequencies), and/or juvenile-onset optic atrophy

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syndrome de Wolfram-like

SNOMEDCT-BE (usually presenting in the first decade of life and principally of low to moderate frequencies), and/or juvenile-onset optic atrophy / 734022008

SNOMEDCT-BE (disorder) / 734022008

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A very rare multisystem neurodegenerative disorder characterized by the presence of eosinophilic intranuclear inclusions in neuronal and glial cells, and neuronal loss. Infantile, juvenile, and adult-onset cases have been described. As any part of th

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maladie des inclusions intranucléaires neuronales

SNOMEDCT-BE (disorder) / 715437003

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Others have searched : familial juvenile gigantomastia juvenile arthritis juvenile bullous pemphigoid juvenile giant cell granuloma juvenile sulfatidosis austin type juvenile Juvenile

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'Juvenile'

Date index:2023-08-21 -

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Translation of "Juvenile " (English → French) :

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Paris - Brussels - Montreal - Genève - Luxembourg - Madrid

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