Clinical and Molecular Characteristics of Japanese Gaucher Disease

@article{Eto1999ClinicalAM,
  title={Clinical and Molecular Characteristics of Japanese Gaucher Disease},
  author={Yoshikatsu Eto and Hiroyuki Ida},
  journal={Neurochemical Research},
  year={1999},
  volume={24},
  pages={207-211}
}
Clinical signs and symptoms of Gaucher disease are more severe in Japanese than in Jewish and other non-Japanese patients. A higher percentage of bone crises and splenectomy was demonstrated by Japanese patients, and there were five fatalities among patients with type 1 Gaucher disease. Additionally, neonatal Gaucher disease, clinically characterized by hydrops foetalis, was observed. Japanese patients with type 2 and type 3 disease also demonstrate clinical heterogeneity. About 100 alleles of… CONTINUE READING
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