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Autosomal dominant disorder
Autosomal dominant inheritance
Autosomal recessive inheritance
Dementia in Huntington's chorea
Recessively inherited

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

autosomal dominant inheritance

transmission autosomique dominante


autosomal dominant inheritance

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


Breast cancer is the most common cancer in women, accounting for 25% of all new cases of cancer. Most cases are sporadic, while 5-10% are estimated to be due to an inherited predisposition. Autosomal dominant alterations in two genes, BRCA1 and BRCA2

syndrome héréditaire de prédisposition au cancer du sein et de l'ovaire


Syndrome with the association of diffuse palmoplantar keratoderma and acrocyanosis. It has been described in eight members of one family and in two sporadic cases. The mode of inheritance in the familial cases was autosomal dominant.

syndrome de kératodermie palmoplantaire diffuse-acrocyanose


autosomal recessive inheritance

transmission autosomique récessive | mode de transmission autosomique récessif | transmission récessive autosomique


Morvan's disease Nelaton's syndrome Sensory neuropathy:dominantly inherited | recessively inherited

Maladie de Morvan Neuropathie sensitive héréditaire à transmission:dominante | récessive | Syndrome de Nélaton


autosomal dominant disorder

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


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


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


Polycystic kidney, autosomal dominant

Rein polykystique, autosomique dominant




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Date index: 2024-02-02
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