Traduction de «lysosomal storage disease » (Anglais → Néerlandais) :

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

lysosomal disease | lysosomal storage disease
lysosomale stapelingsziekte

An extremely rare genetic glycogen storage disease reported in one patient to date. Clinical signs included muscle weakness, cardiac arrhythmia associated with accumulation of abnormal storage material in the heart and glycogen depletion in skeletal
glycogeenstapelingsziekte type 15

Myopathy in:glycogen storage disease (E74.0+) | lipid storage disorders (E75.-+)
myopathie bij | glycogeenstapelingsziekten (E74.0) | myopathie bij | vetstapelingsziekten (E75.-)

A genetically inherited anomaly of glycogen metabolism and a form of glycogen storage disease characterized by fasting hypoglycemia. It is an extremely rare disease; about 20 cases have been reported in the literature so far. The disease appears in i
levergebonden glycogeensynthasedeficiëntie

acid maltase deficiency | glycogen storage disease type II | glycogenosis type II | Pompe disease | AMD [Abbr.] | GSD-II [Abbr.]
ziekte van Pompe

Renal tubulo-interstitial disorders in:cystinosis (E72.0+) | glycogen storage disease (E74.0+) | Wilson's disease (E83.0+)
tubulo-interstitiële nieraandoeningen bij | cystinose (E72.0) | tubulo-interstitiële nieraandoeningen bij | glycogeenstapelingsziekte (E74.0) | tubulo-interstitiële nieraandoeningen bij | ziekte van Wilson (E83.1)

Glycogen storage disease
glycogeenstapelingsziekte

storage disease
bewaarziekte