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A.-F.syndrome
AMD
Abderhalden-Fanconi syndrome
Accumulation disease
Acid maltase deficiency
Amylopectinosis
Amylopectinosis brancher deficiency
Andersen disease
Andersen's disease
Brancher deficiency
Brancher enzyme deficiency
Cystine storage disease
Cystinosis
Dextrinosis
Familia
GSD IV
GSD-II
Gierke's 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
Lignac-Fanconi syndrome
Lysosomal disease
Lysosomal storage disease
Najjar-Andersen syndrome
Pompe disease
Storage disease
Thesaurismosis
Thesaurisomsis
Thesaurosis
Type 1 glycogenosis
Type I glycogen storage disease
Von Gierke's disease

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

A.-F.syndrome | cystine storage disease

diabète rénal gluco-phosphoaminé | syndrome de De Toni-Debré-Fanconi


cystinosis | cystine storage disease | Abderhalden-Fanconi syndrome | Lignac-Fanconi syndrome

cystinose | maladie de Lignac-Fanconi


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 ]


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


lysosomal disease | lysosomal storage disease

déficit du stockage lysosomal | maladie lysosomiale


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 ]


thesaurismosis | accumulation disease | storage disease | thesaurisomsis | thesaurosis

thésaurismose


glycogen storage disease | glycogenosis | glycogenopathy | dextrinosis | glycogenoses

glycogénose | thésaurose glycogénique | glycogénoses


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