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@proceedings{1351739,
author = {Kosinová, Martina and Štourač, Petr and Voháňka, Stanislav and Huser, Martin},
booktitle = {Euroanaesthesia 2016},
keywords = {Becker myotonia; Anaesthetic management; sugammdex},
language = {eng},
title = {Anaesthetic management of a parturient with becker’s myotonia congenita using propofol, rocuronium and sugammadex.},
year = {2016}
}
TY - CONF
ID - 1351739
AU - Kosinová, Martina - Štourač, Petr - Voháňka, Stanislav - Huser, Martin
PY - 2016
TI - Anaesthetic management of a parturient with becker’s myotonia congenita using propofol, rocuronium and sugammadex.
KW - Becker myotonia
KW - Anaesthetic management
KW - sugammdex
N2 - Becker’s Disease is an autosomal recessive type of myotonia congenita. Worldwide prevalence is about 1/100000. It is linked to mutations in CLCN1, the gene encoding skeletal muscle chloride channel. It reduces flow of chloride ions during repolarization and leads to sustained muscle contractions. Typical clinical symptoms are myotonic stiffness and “warm-up” phenomenon.
ER -
KOSINOVÁ, Martina, Petr ŠTOURAČ, Stanislav VOHÁŇKA a Martin HUSER. Anaesthetic management of a parturient with becker’s myotonia congenita using propofol, rocuronium and sugammadex. In \textit{Euroanaesthesia 2016}. 2016. ISSN~0265-0215.
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