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Translation of "cerebellar tonsil " (English → French) :

Arnold-Chiari malformation | cerebellar ectopia | Chiari malformation | herniation of the cerebellar tonsils | hindbrain herniation

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malformation d'Arnold-Chiari

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amygdala of cerebellum | tonsilla of cerebellum | cerebellar tonsil

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]

This syndrome has characteristics of short stature, anterior pituitary hormone deficiency, small sella turcica and a hypoplastic anterior hypophysis associated with pointed cerebellar tonsils. It has been described in three generations of large Frenc

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syndrome de petite taille-anomalies hypophysaires et cérébelleuses-selle turcique anormale

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http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

tonsille pharyngienne | amygdale pharyngée | amygdale de Luschka | glande de Luschka | amygdale pharyngienne

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]

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amygdale pharyngienne [ amygdale pharyngée de Luschka | amygdale | amygdale pharyngée | tonsilla pharyngealis | tonsilla pharyngea ]

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http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]

cryptic tonsillitis | follicular tonsillitis | lacunar tonsillitis

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angine folliculaire | angine lacunaire | angine pultacée

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tubal tonsil | eustachian tonsil | Gerlach's tonsil

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

tonsille tubaire | amygdale tubaire | amygdale de la trompe | amygdale de Gerlach

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]

palatine tonsil | pharyngeal tonsil

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amygdale pharyngienne

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Cerebellar ataxia Cayman type has characteristics of psychomotor retardation, hypotonia and cerebellar dysfunction (nystagmus, ataxic gait, truncal ataxia, dysarthric speech and intention tremor), associated with cerebellar hypoplasia. The prevalence

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ataxie type Caïman

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A very rare subtype of autosomal dominant cerebellar ataxia type 3 with characteristics of late-onset and slowly progressive cerebellar signs (gait ataxia) and eye movement abnormalities. To date, only 23 affected patients have been described from on

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ataxie spinocérébelleuse type 26

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datacenter (1): www.wordscope.ca (v4.0.br)

'cerebellar tonsil' ->

Date index: 2022-01-15