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Neuronopathic Gaucher disease (nGD) has a very wide clinical and genotypic spectrum. However, there is no consensus definition of nGD, including no description of how best to diagnostically separate the acute form-Gaucher type 2-from the subacute or chronic form-Gaucher type 3. In this article, we define the various forms of Gaucher disease with particular emphasis on the presence of gaze palsy in all patients with nGD. This consensus definition will help in both clinical diagnosis and appropriate patient recruitment to upcoming clinical trials. © 2020 The Authors. Journal of Inherited Metabolic Disease published by John Wiley & Sons Ltd on behalf of SSIEM.

Citation

Raphael Schiffmann, Jeff Sevigny, Arndt Rolfs, Elin Haf Davies, Ozlem Goker-Alpan, Magy Abdelwahab, Ashok Vellodi, Eugen Mengel, Elena Lukina, Han-Wook Yoo, Tanya Collin-Histed, Aya Narita, Tama Dinur, Shoshana Revel-Vilk, David Arkadir, Jeff Szer, Michael Wajnrajch, Uma Ramaswami, Ellen Sidransky, Aimee Donald, Ari Zimran. The definition of neuronopathic Gaucher disease. Journal of inherited metabolic disease. 2020 Sep;43(5):1056-1059

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PMID: 32242941

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