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PLoS Curr. 2012 Feb 15;4:RRN1304. doi: 10.1371/currents.RRN1304.

Current Pharmacological Management in Juvenile Huntington's Disease.

PLoS currents

Lisa Robertson, Helen Santini, Kirsty L O'Donovan, Ferdinando Squitieri, Roger A Barker, Maria Rakowicz, G Bernhard Landwehrmeyer, Oliver Quarrell

Affiliations

  1. Department of Clinical Genetics, Sheffield Children's Hospital, Sheffield UK S10 2TH; Neurogenetics and Rare Diseases Centre, IRCCS Neuromed, Pozzilli (IS), Italy.; University of Cambridge; Department of Clinical Neurophysiology, Institute of Psychiatry and Naurology, Warsaw, Poland and Dept. of Neurology, University of Ulm, Ulm, Germany.

PMID: 22474619 PMCID: PMC3283037 DOI: 10.1371/currents.RRN1304

Abstract

BACKGROUND: The clinical presentation of Juvenile Huntington's Disease (JHD) can be very different from adult-onset HD with little evidence to guide symptomatic management.

AIM: To survey the current use of pharmacological treatments for JHD.

METHODS: Patients were identified through the HD Association, Hospital Doctors and the European Huntington's Disease Network REGISTRY study.

RESULTS: The most commonly prescribed agents were anti-psychotics (24/45), anti-depressants (17/45) and anti-parkinsonian medications (15/45). 5 patients were taking more than 8 medications.

CONCLUSIONS: The most commonly prescribed group of medication was the anti-psychotic. Many patients were on multiple therapies, highlighting the need to rationalise medications.

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