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AMD
Acid maltase deficiency
Amylopectinosis
Amylopectinosis brancher deficiency
Andersen disease
Andersen's disease
Basedow's disease
Blue disease
Blue ear disease
Blue-ear disease of pigs
Brancher deficiency
Brancher enzyme deficiency
Exophthalmic goiter
Familia
Flajani's disease
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
Glycogenosis
Glycogenosis IV
Glycogenosis type II
Graves disease
Graves's disease
Hepatorenal glycogenosis
MSD
March's disease
Mysterious pig disease
Mysterious swine disease
Mystery pig disease
Najjar-Andersen syndrome
New pig disease
PRRS
Parry disease
Parry's disease
Pompe disease
Porcine epidemical abortion
Porcine reproductive and respiratory syndrome
Purple ears disease
Stokes's disease
Thyrotoxicosis
Type 1 glycogenosis
Type I glycogen storage disease
Von Gierke's disease
Wilson's disease

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

glycogen storage disease [ glycogen disease | glycogenosis ]

glycogénose


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 ]


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 ]


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


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


blue disease | blue ear disease | blue-ear disease of pigs | mysterious pig disease | mysterious swine disease | mystery pig disease | new pig disease | porcine epidemical abortion | porcine reproductive and respiratory syndrome | purple ears disease | MSD [Abbr.] | PRRS [Abbr.]

maladie bleue | maladie de l'oreille bleue | maladie mystérieuse du porc | mystérieuse maladie des porcs | nouvelle maladie des porcs | nouvelle maladie du porc | syndrome affectant la reproduction et la respiration chez les porcs | syndrome dysgénésique et respiratoire du porc | MMP [Abbr.] | SDRP [Abbr.]


Basedow's disease | exophthalmic goiter | Flajani's disease | Graves disease | Graves's disease | March's disease | Parry disease | Parry's disease | Stokes's disease | thyrotoxicosis

goitre exophtalmique | maladie de Basedow | maladie de Flajani | maladie de Graves | maladie de Marsh


Disease with characteristics of the adult-onset (average age 40 years) of truncal ataxia, gait disturbance and gaze-evoked nystagmus. The disease is slowly progressive with dysarthria and limb ataxia following. Additional manifestations include diplo

ataxie spinocérébelleuse type 38


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