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AMD
Acid maltase deficiency
GSD-II
Glycogen storage disease
Glycogen storage disease
Glycogen storage disease type II
Glycogenosis type II
Lipid storage disorders
Myopathy in glycogen storage disease
Pompe disease
Wilson's disease

Vertaling van "Myopathy in glycogen storage disease " (Engels → Nederlands) :

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

myopathie bij | glycogeenstapelingsziekten (E74.0) | myopathie bij | vetstapelingsziekten (E75.-)


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


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)




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

volwassen polyglucosan body-ziekte




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'Myopathy in glycogen storage disease ' ->

Date index: 2022-12-16
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