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Choroideremia
Degeneration of iris
Dementia in Huntington's chorea
Progressive chorioretinal degeneration
Progressive choroidal atrophy
Progressive neuronal degeneration with liver cirrhosis
Progressive pyramido-pallidal degeneration
Progressive tapetochoroidal atrophy
Progressive tapetochoroidal dystrophy
Pupillary margin
Tapetochoroidal dystrophy

Vertaling van "Progressive chorioretinal degeneration " (Engels → Frans) :

choroideremia [ tapetochoroidal dystrophy | progressive tapetochoroidal dystrophy | progressive choroidal atrophy | progressive tapetochoroidal atrophy | progressive chorioretinal degeneration ]

choroïdérémie [ dégénérescence chorio-rétinienne progressive ]


Progressive neuronal degeneration with liver cirrhosis

poliodystrophie sclérosante progressive


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

ataxie spinocérébelleuse type 28


An early-onset chorioretinal dystrophy with characteristics of large atrophic macular and nasal retinal lesions, nystagmus, myopia, poor vision and slow disease progression. It has been described in two large families. Transmission is autosomal domin

atrophie bifocale choriorétinienne progressive


progressive pyramido-pallidal degeneration

dégénérescence pyramido-pallidale progressive


Degeneration of:iris (pigmentary) | pupillary margin | Iridoschisis Iris atrophy (essential)(progressive) Miotic pupillary cyst Translucency of iris

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


Definition: A dementia occurring as part of a widespread degeneration of the brain. The disorder is transmitted by a single autosomal dominant gene. Symptoms typically emerge in the third and fourth decade. Progression is slow, leading to death usually within 10 to 15 years. | Dementia in Huntington's chorea

Définition: Démence survenant dans le contexte d'une dégénérescence cérébrale étendue. La maladie est transmise par un gène autosomique dominant unique. Les symptômes apparaissent typiquement dans la troisième et la quatrième décennies. L'évolution est lentement progressive, aboutissant habituellement à la mort en 10 à 15 années. | Démence de la chorée de Huntington




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Date index: 2023-11-19
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