Harp Syndrome
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.
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| Format: | Article |
| Language: | English |
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Pediatric Neurology Briefs Publishers
1995-04-01
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| Series: | Pediatric Neurology Briefs |
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| Online Access: | https://www.pediatricneurologybriefs.com/articles/2608 |
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