Literature DB >> 26329151

[Gaucher Disease].

Torayuki Okuyama1.   

Abstract

Gaucher disease is an autosomal recessive disorder caused by congenital deficiency of lysosomal glucocerebrosidase. Gaucher disease is classified into three types. In addition to enzyme replacement therapy, substrate reduction therapy, chemical chaperon therapy, and hematopoietic stem cell transplantation therapy are considered for the effective treatment of Gaucher disease.

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Year:  2015        PMID: 26329151     DOI: 10.11477/mf.1416200267

Source DB:  PubMed          Journal:  Brain Nerve        ISSN: 1881-6096


  1 in total

1.  A novel mutation causing type 1 Gaucher disease found in a Japanese patient with gastric cancer: A case report.

Authors:  Sakura Hosoba; Katsuyuki Kito; Yukako Teramoto; Kaori Adachi; Ryota Nakanishi; Ai Asai; Masaki Iwasa; Rie Nishimura; Suzuko Moritani; Masahiro Kawahara; Hitoshi Minamiguchi; Eiji Nanba; Ryoji Kushima; Akira Andoh
Journal:  Medicine (Baltimore)       Date:  2018-07       Impact factor: 1.889

  1 in total

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