Traduction de «Glycogen storage disease » (Anglais → Français) :

type I glycogen storage disease [ von Gierke's disease | Gierke's disease | type 1 glycogenosis | glycogen storage disease I | hepatorenal glycogenosis ]
maladie de von Gierke [ glycogénose de type I | glycogénose hépato-rénale ]

glycogen storage disease [ glycogen disease | glycogenosis ]
glycogénose

A glycogen storage disease of adults with characteristics of progressive upper and lower motor neuron dysfunction, progressive neurogenic bladder and cognitive difficulties that can lead to dementia. The prevalence is unknown. More than 50 cases have
maladie des corps de polyglucosane de l'adulte

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
glycogénose avec cardiomyopathie sévère par déficit en glycogénine

acid maltase deficiency | glycogen storage disease type II | glycogenosis type II | Pompe disease | AMD [Abbr.] | GSD-II [Abbr.]
déficit en maltase acide | glycogénose de type II | maladie de Pompe | GSD II [Abbr.]

Myopathy in:glycogen storage disease (E74.0+) | lipid storage disorders (E75.-+)
Myopathie au cours d'anomalies de stockage (du) (des):glycogène (E74.0+) | lipides (E75.-+)

Andersen's disease [ Andersen disease | Najjar-Andersen syndrome | glycogenosis IV | glycogen storage disease type IV | GSD IV | alpha 1,4-glucan-6-glucosyl transferase deficiency | amylopectinosis brancher deficiency | brancher enzyme deficiency | brancher deficiency | amylopectinosis | familia ]
maladie d'Andersen [ glycogénose musculaire type IV ]

lysosomal disease | lysosomal storage disease
déficit du stockage lysosomal | maladie lysosomiale

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

storage disease
maladie d'entreposage