Contribution to the clinical polymorphism in Huntington's disease
Motta, E.; Filipowicz, A.; Rościszewska, D.; Gabryś, E.
Neurologia i Neurochirurgia Polska 26(6): 873-877
1992
ISSN/ISBN: 0028-3843 PMID: 1301515 Document Number: 395240
A family is described in which closely consanguineous parents had Huntington chorea and in their son a severe hypertonic-hypokinetic syndrome with pellagra-like cutaneous changes was present. In two generations of the family in 6 subjects involuntary movements and gait disorders were reported.
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