Harp Syndrome

J Gordon Millichap

doi:10.15844/pedneurbriefs-9-4-3

Harp Syndrome

Pediatric Neurology Briefs

Volume 9 (1995): Issue 4

By: J Gordon Millichap

Open Access

|Apr 1995

Abstract

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.

References

Orrell RW Amrolia RJ Heald A Cleland PG Owen JS Morgan-Hughes JA Acanthocytosis, retinitis pigmentosa, and pallidal degeneration: A report of three patients, including the second reported case with hypoprebetalipoproteinemia (HARP syndrome) Neurology 1995 Mar 45 3 Pt 1 487 492 7898702
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-9-4-3 | Journal eISSN: 2166-6482

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Language: English

Page range: 26 - 27

Published on: Apr 1, 1995

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Harp Syndrome,

Dysphagia,

Orobucco-Lingual Dystonia

© 1995 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 9 (1995): Issue 4