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Parkinson disease in Gaucher disease.
BACKGROUND: Gaucher disease (GD) is an inborn error of metabolism caused by mutations in the gene ( GBA ) coding for glucocerebrosidase (GCase), inherited in an autosomal recessive pattern. GD patients have up to 9% risk of developing PD.
CASE PRESENTATION: We report two patients with GD that developed PD at different disease stages.
CONCLUSION: We reviewed the literature on the coexistence of PD and GD and speculate that the severity of symptoms may be related to the type of GBA mutation inherited.
CASE PRESENTATION: We report two patients with GD that developed PD at different disease stages.
CONCLUSION: We reviewed the literature on the coexistence of PD and GD and speculate that the severity of symptoms may be related to the type of GBA mutation inherited.
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