Traduction de «Hepatolenticular degeneration » (Anglais → Néerlandais) :

hepatolenticular degeneration | Wilson disease | Wilson syndrome
hepatolenticulaire degeneratie | ziekte van Wilson

Dementia in:cerebral lipidosis (E75.-+) | epilepsy (G40.-+) | hepatolenticular degeneration (E83.0+) | hypercalcaemia (E83.5+) | hypothyroidism, acquired (E01.-+, E03.-+) | intoxications (T36-T65+) | multiple sclerosis (G35+) | neurosyphilis (A52.1+) | niacin deficiency [pellagra] (E52+) | polyarteritis nodosa (M30.0+) | systemic lupus erythematosus (M32.-+) | trypanosomiasis (B56.-+, B57.-+) | vitamin B12 deficiency (E53.8+)
dementie bij | epilepsie (G40.-) | dementie bij | hepatolenticulaire degeneratie (E83.0) | dementie bij | hersenlipidose (E75.-) | dementie bij | hypercalciëmie (E83.5) | dementie bij | hypothyroïdie, verworven (E01.-, E03.-) | dementie bij | intoxicaties (T36-T65) | dementie bij | lupus erythematodes disseminatus (M32.-) | dementie bij | multipele sclerose (G35) | dementie bij | neurosyfilis (A52.1) | dementie bij | niacinedeficiëntie [pellagra] (E52) | dementie bij | polyarteriitis nodosa (M30.0) | dementie bij | trypanosomiasis (B56.-, B57.-) | dementie bij | uremie (N18.5) | dementie bij | vitamine B12-deficiëntie (E53.8)

hepatolenticular
hepatolenticulair

age-related macular degeneration | senile macular degeneration | AMD [Abbr.] | ARMD [Abbr.]
ouderdomsmaculadegeneratie

corrosion conditions | degeneration and oxidising varieties | corrosion types | degeneration and oxidising categories
soorten corrosie

Alcoholic:cerebellar:ataxia | degeneration | cerebral degeneration | encephalopathy | Dysfunction of autonomic nervous system due to alcohol
alcoholische | cerebellaire | ataxie | alcoholische | cerebellaire | degeneratie | alcoholische | cerebrale degeneratie | alcoholische | encefalopathie | disfunctie van autonoom zenuwstelsel door alcoholgebruik

Angioid streaks | Cyst | Drusen (degenerative) | Hole | Puckering | of macula | Kuhnt-Junius degeneration Senile macular degeneration (atrophic)(exudative) Toxic maculopathy
angioïde strepenvan macula | cystevan macula | drusen (degeneratief)van macula | gatvan macula | macular pucker | Kuhnt-Junius-degeneratie | seniele maculadegeneratie (atrofisch)(exsudatief) | toxische maculopathie

A rare hereditary motor and sensory neuropathy with characteristics of intermediate motor median nerve conduction velocities (usually between 25 and 45 m/s) and signs of both demyelination and axonal degeneration in nerve biopsies. It presents with m
autosomaal dominante intermediaire ziekte van Charcot-Marie-Tooth type B

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
spinocerebellaire ataxie type 28

A rare hereditary motor and sensory neuropathy with characteristics of intermediate motor median nerve conduction velocities (usually between 25 and 45 m/s) and signs of both axonal degeneration and demyelination without onion bulbs in nerve biopsies
autosomaal dominante intermediaire ziekte van Charcot-Marie-Tooth type D