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AMD
Acid maltase deficiency
Amylopectinosis
Amylopectinosis brancher deficiency
Andersen disease
Andersen's disease
Brancher deficiency
Brancher enzyme deficiency
Dextrinosis
Familia
GSD IV
GSD-II
Gierke's disease
Glycogen disease
Glycogen storage disease
Glycogen storage disease
Glycogen storage disease I
Glycogen storage disease type II
Glycogen storage disease type IV
Glycogenopathy
Glycogenoses
Glycogenosis
Glycogenosis IV
Glycogenosis type II
Hepatorenal glycogenosis
Lipid storage disorders
Myopathy in glycogen storage disease
Najjar-Andersen syndrome
Pompe disease
Type 1 glycogenosis
Type I glycogen storage disease
Von Gierke's disease
Wilson's disease

Traduction de «genetic glycogen storage » (Anglais → Français) :

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


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 ]


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.-+)


glycogen storage disease [ glycogen disease | glycogenosis ]

glycogénose


Renal tubulo-interstitial disorders in:cystinosis (E72.0+) | glycogen storage disease (E74.0+) | Wilson's disease (E83.0+)

Maladie rénale tubulo-interstitielle au cours de:cystinose (E72.0+) | glycogénose (E74.0+) | maladie de Wilson (E83.0+)


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




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.]


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 ]


glycogen storage disease | glycogenosis | glycogenopathy | dextrinosis | glycogenoses

glycogénose | thésaurose glycogénique | glycogénoses




datacenter (1): www.wordscope.fr (v4.0.br)

'genetic glycogen storage' ->

Date index: 2022-08-26
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