A genome wide search for susceptibility loci in three European malignant hyperthermia pedigrees

R L Robinson, N Monnier, W Wolz, M Jung, A Reis, G Nuernberg, J L Curran, K Monsieurs, P Stieglitz, L Heytens, R Fricker, C van Broeckhoven, T Deufel, P M Hopkins, J Lunardi, C R Mueller

Publikation: Beitrag in FachzeitschriftArtikelBegutachtung

Abstract

Malignant hyperthermia (MH) is an autosomal dominant disorder which is potentially lethal in susceptible individuals on exposure to commonly used inhalational anaesthetics and depolarising muscle relaxants. Crises reflect the consequences of disturbed skeletal muscle calcium homeostasis. Susceptibility was first localised to chromosome 19q13.1 and the skeletal muscle ryanodine receptor, RYR1 (the calcium release channel of the sarcoplasmic reticulum). Defects in this gene have been identified which cosegregate with the MHS phenotype and evidence as to their potential causal roles has accumulated. MH has, however, been shown to be genetically heterogeneous, additional loci on chromosomes 3q, 17q and 7q being proposed. Pedigrees remain in Europe where linkage status is still unclear. In a collaborative search of the human genome conducted with three pedigrees whose disease status was classified according to the European IVCT protocol we have evidence to suggest that at least two further loci exist for MH susceptibility. One of these locates to chromosome 1q, the site of a candidate gene, CACNL1A3, encoding the alpha-subunit of the dihydropyridine receptor. The second region resides on chromosome 5p to where no known candidate has been mapped to date. The third family exhibited inconclusive results which suggests the existence of at least one other locus. This study adds to the evidence for considerable genetic heterogeneity in MH and will provide a route to further our understanding of the molecular pathology of the condition.

OriginalspracheEnglisch
Seiten (von - bis)953-61
Seitenumfang9
FachzeitschriftHuman Molecular Genetics
Volume6
Issue6
DOIs
PublikationsstatusVeröffentlicht - Juni 1997

Research Field

  • Molecular Diagnostics

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