Harp Syndrome
DOI:
https://doi.org/10.15844/pedneurbriefs-9-4-3Keywords:
Harp Syndrome, Dysphagia, Orobucco-Lingual DystoniaAbstract
Harp syndrome, characterized by hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration, is described in three patients from the National Hospital, Queen Square, London, Newcastle General Hospital, and the Royal Free Hospital, London, UK.Published
1995-04-01
Issue
Section
Degenerative Diseases
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Copyright (c) 1995 The Author(s)
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