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10.3390/diseases5010010

http://scihub22266oqcxt.onion/10.3390/diseases5010010
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C5456331!5456331!28933363
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suck abstract from ncbi


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pmid28933363      Diseases 2017 ; 5 (1): ä
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  • The Spectrum of Neurological Manifestations Associated with Gaucher Disease #MMPMID28933363
  • Roshan Lal T; Sidransky E
  • Diseases 2017[Mar]; 5 (1): ä PMID28933363show ga
  • Gaucher disease, the most common lysosomal storage disorder, is due to a deficiency in the enzyme glucocerebrosidase. This leads to the accumulation of its normal substrate, glucocerebroside, in tissue macrophages, affecting the hematological, visceral, bone and neurologic systems. Gaucher disease is classified into three broad phenotypes based upon the presence or absence of neurological involvement: type 1 (non-neuronopathic), type 2 (acute neuronopathic), and type 3 (subacute neuronopathic). Phenotypically, there is a wide spectrum of visceral and neurological manifestations. Enzyme replacement is effective in managing the visceral disease; however, treating the neurological manifestations has proved to be more challenging. This review discusses the various neurological manifestations encountered in Gaucher disease, and provides a brief overview regarding the treatment and ongoing research challenges.
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