Gaucher Disease Type IIIC, with Oculomotor Apraxia
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.
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| Format: | Article |
| Language: | English |
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Pediatric Neurology Briefs Publishers
2000-01-01
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| Series: | Pediatric Neurology Briefs |
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| Online Access: | https://www.pediatricneurologybriefs.com/articles/1968 |