Gaucher Disease Type IIIC, with Oculomotor Apraxia
Abstract
Four siblings with consanguineous parents, presenting with oculomotor apraxia in early childhood, were diagnosed with Gaucher disease (GD) at 10 years of age, at King Faisal Specialist Hospital, Riyadh, Saudi Arabia.
DOI: https://doi.org/10.15844/pedneurbriefs-14-1-8 | Journal eISSN: 2166-6482
Language: English
Page range: 8 - 8
Published on: Jan 1, 2000
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
© 2000 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.