Leitlinien Chorea/Morbus Huntington für die deutschsprachigen Länder neu überarbeitet

Translated title of the contribution: Guidelines Chorea/Huntington Disease for the German-Speaking Countries Revised

Carsten Saft, Raphael M. Bonelli, Jean Marc Burgunder, Matthias Dose, Jörg T. Epplen, Hans H. Jung, Josef Priller, Ralf Reilmann, Sabine Rudnik, Klaus Seppi, G. Bernhard Landwehrmeyer

Research output: Contribution to journalReview articlepeer-review

2 Scopus citations

Abstract

The updated and revised guidelines (S2k level) on 'Chorea and Huntington's Disease (HD)' review the present understanding of the natural history of HD including rate of progression and describe new approaches to symptomatic and disease course-modifying therapies in HD. In contrast to other guidelines, the expert opinion in the German speaking countries favors tiapride as a first line treatment of chorea. Because of the side effect profile of tetrabenazine, including depression or akathisia, the authors prefer to use tetrabenazine as second line treatment. The current guidelines address medico-legal aspects of preimplantation genetic diagnosis (PGD) and prenatal testing in Germany, Austria and Switzerland as well as differences between a predictive and a diagnostic setting of molecular genetic diagnosis. In addition, the guidelines comment in detail on the differential diagnoses of a chorea of unknown origin.

Translated title of the contributionGuidelines Chorea/Huntington Disease for the German-Speaking Countries Revised
Original languageGerman
Pages (from-to)570-585
Number of pages16
JournalAktuelle Neurologie
Volume45
Issue number8
DOIs
StatePublished - 2018
Externally publishedYes

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