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Familial dyslexia: genetic and medical findings in eleven three-generation families

✍ Scribed by Herbert A. Lubs; Mark Rabin; Esther Feldman; Bonnie J. Jallad; Alexander Kushch; Karen Gross-Glenn; Ranjan Duara; R. C. Elston


Book ID
112941258
Publisher
Springer US
Year
1993
Tongue
English
Weight
748 KB
Volume
43
Category
Article
ISSN
0736-9387

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## Abstract Chorea‐acanthocytosis is a rare autosomal recessive disorder. Its characteristics are orofacial dyskinesia, hyporeflexia, seizures, aberrant behavior, atrophy of the caudate and putamen, and acanthocytes in the blood with a normal level of lipoproteins. We describe three families with c