HARP Syndrome

J Gordon Millichap

doi:10.15844/pedneurbriefs-6-2-1

HARP Syndrome

Pediatric Neurology Briefs

Volume 6 (1992): Issue 2

By: J Gordon Millichap

Open Access

|Feb 1992

Abstract

The clinical and laboratory studies of an 11 year old girl with hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa and pallidal degeneration are reported from the Developmental and Metabolic Neurology Branch, National Institute of Neurological Disorders and Stroke and Clinical Pathology Department, National Institutes of Health, Bethesda, MD.

References

Higgins JJ Patterson MC Papadopoulos NM Brady RO Pentchev PG Barton NW Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration (HARP syndrome) Neurology 1992 Jan 42 1 194 198 10.1212/WNL.42.1.194 1734303
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Swisher CN Menkes JH Cancilla PA Dodge PR Trans Am Neurol Assoc 1972 97 212
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Feinberg TE Cianci CD Morrow JS Pehta JC Redman CM Huima T Diagnostic tests for choreoacanthocytosis Neurology 1991 Jul 41 7 1000 1006 10.1212/WNL.41.7.1000 1829792
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-6-2-1 | Journal eISSN: 2166-6482

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Language: English

Page range: 9 - 9

Published on: Feb 1, 1992

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Hypoprebetalipoproteinemia,

Acanthocytosis,

Retinitis Pigmentosa

© 1992 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 6 (1992): Issue 2