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ARPKD
Autosomal dominant brachyolmia
Autosomal dominant disorder
Autosomal dominant inheritance
Autosomal dominant mode
Autosomal dominant polycystic kidney disease
CADASIL
CADASIL disease
Congenital polycystic disease
Dementia in Huntington's chorea
Hereditary multi-infarct type dementia
Polycystic kidney disease

Traduction de «Autosomal dominant disorder » (Anglais → Français) :

autosomal dominant disorder

maladie héréditaire dominante autosomique | maladie autosomique dominante | maladie dominante autosomique


A rare benign autosomal dominant disorder of fat tissue proliferation with characteristic of presence of multiple small lipomas of 2 to 5 cm in diameter in the middle third of the body (i.e. the forearms, trunk, and upper thighs), and which are gener

lipomatose mésosomatique de Roch-Leri


CADASIL | CADASIL disease | cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy | hereditary multi-infarct type dementia

CADASIL | syndrome CADASIL


autosomal dominant inheritance

transmission autosomique dominante


autosomal dominant polycystic kidney disease | congenital polycystic disease | polycystic kidney disease | ARPKD [Abbr.]

polykystose rénale | PKR [Abbr.]


autosomal dominant inheritance

mode de transmission autosomique dominant | hérédité dominante | hérédité dominante autosomique | transmission autosomique dominante




Autosomal dominant brachyolmia (disorder)

brachyolmie type 3


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


An autosomal dominant form of hereditary motor and sensory neuropathy with dominant proximal involvement. Manifestations include adult-onset proximal neurogenic atrophy, sensory involvement, painful muscle cramps, fasciculations, areflexia, and high

neuropathie sensitivo-motrice héréditaire type Okinawa




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Date index: 2022-09-07
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