Traduction de «autosomal dominant keratitis » (Anglais → Néerlandais) :

Autosomal dominant keratitis
autosomaal dominante keratitis

Hereditary mixed polyposis syndrome (HMPS) describes an autosomal dominantly inherited large-bowel disease with characteristics of the presence of a mixture of hyperplastic, atypical juvenile and adenomatous polyps that are associated with an increas
hereditary mixed polyposis syndrome

autosomal dominant polycystic kidney disease | congenital polycystic disease | polycystic kidney disease | ARPKD [Abbr.]
cystennier | polycystose renis | polycystosis renis | ren cysticus

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
erfelijke motorische en sensorische neuropathie, Okinawa-type

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
Omschrijving: Een dementie die optreedt als onderdeel van een uitgebreide degeneratie van de hersenen. De stoornis vererft via een enkel autosomaal dominant gen. Typerend is het manifest worden van de symptomen in de derde en vierde decade. Progressie is langzaam, gewoonlijk in 10 tot 15 jaar tot de dood leidend. | Neventerm: | dementie bij chorea van Huntington

Polycystic kidney, autosomal dominant
polycystische nier, autosomaal dominant