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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 and 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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