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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Autor principal: J Gordon Millichap (Autor)
Formato: Livro
Publicado em: Pediatric Neurology Briefs Publishers, 2000-01-01T00:00:00Z.
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3rd Floor Main Library

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Número de Chamada: A1234.567
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