British Journal of Anaesthesia, Vol 79, Issue 3 332-337, Copyright © 1997 by The Board of Management and Trustees of the British Journal of Anaesthesia
K. A. Quane, H. Ording, K. E. Keating, B. M. Manning, R. Heine, D. Bendixen, K. Berg, R. Krivosic-Horber, F. Lehmann-Horn, T. Fagerlund and T. V. McCarthy
Malignant hyperthermia (MH) is a potentially fatal autosomal dominant
disorder of skeletal muscle and is triggered in susceptible people by all
commonly used inhalation anaesthetics and depolarizing neuromuscular
blocking agents. To date, eight mutations in the skeletal muscle ryanodine
receptor gene (RYR1) have been identified in malignant hyperthermia
susceptible (MHS) and central core disease (CCD) cases. We have screened
the RYR1 gene in affected individuals for novel MHS mutations by single
stranded conformational polymorphism (SSCP) analysis and have identified a
G to T transition mutation which results in the replacement of a conserved
arginine (Arg) at position 614 with a leucine (Leu). The Arg614Leu mutation
was present in three unrelated MHS individuals of 151 investigated. The
mutation was not detected in 148 normal chromosomes and segregated
precisely with MHS in family members from one of the probands where DNA was
available for analysis. This mutation occurs at the same position as the
previously identified Arg to Cys mutation reported in all cases of porcine
MH and in approximately 5% of human MH. A comparison of the phenotypes of
the Arg614Leu and Arg614Cys probands is presented.
CLINICAL INVESTIGATIONS
Detection of a novel mutation at amino acid position 614 in the ryanodine receptor in malignant hyperthermia
Department of Biochemistry, University College, Cork, Ireland; Herlev Hospital, University of Copenhagen, Herlev Ringvej 75, DK 2730, Herlev, Denmark; Department of Applied Physiology, University of Ulm, Albert Einstein Allee 11, D-89069 Ulm, Federal Republic of Germany; Department of Anaesthesia, Ulleval University Hospital, Kirkeveien 166, N-0407 Oslo, Norway; Malignant Hyperthermia Unit, Hospital B, CHRU de Lille 59037, Lille Cedex, France
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