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.

Bibliographic Details
Main Author: J Gordon Millichap
Format: Article
Language:English
Published: Pediatric Neurology Briefs Publishers 2000-01-01
Series:Pediatric Neurology Briefs
Subjects:
Online Access:https://www.pediatricneurologybriefs.com/articles/1968
Description
Summary: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.
ISSN:1043-3155
2166-6482