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Cornea Transplant Act
Corneal degeneration
Degeneration of the cornea
Degeneration of the dental pulp
Dementia in Huntington's chorea
Lipoid degeneration of the liver
Marginal degeneration of the cornea
Recidivating erosion of the cornea
Recurring erosion of the cornea
Terrien's disease
Terrien's marginal degeneration

Traduction de «degeneration the cornea » (Anglais → Français) :

corneal degeneration [ degeneration of the cornea ]

dégénérescence cornéenne


marginal degeneration of the cornea [ Terrien's disease | Terrien's marginal degeneration ]

dégénérescence marginale de Terrien


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


recidivating erosion of the cornea | recurring erosion of the cornea

érosion récidivante de la cornée


Cornea Transplant Act [ An Act to Facilitate Cornea Transplants from the Bodies of Deceased Persons to Living Persons ]

Cornea Transplant Act [ An Act to Facilitate Cornea Transplants from the Bodies of Deceased Persons to Living Persons ]


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


A lysosomal storage disease with clinical characteristics of psychomotor retardation and visual abnormalities including corneal clouding, retinal degeneration or strabismus. The disease is rare in the general population but is more prevalent among As

mucolipidose type IV


A rare genetic central nervous system malformation syndrome characterized by bilateral congenital cataracts and severe hemorrhagic destruction of the brain parenchyma with associated massive cystic degeneration, enlarged ventricles and subependymal c

syndrome de porencéphalie-microcéphalie-cataracte bilatérale congénitale


degeneration of the dental pulp

dégénérescence de la pulpe dentaire


Lipoid degeneration of the liver

dégénérescence lipoïde




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Date index: 2023-09-16
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