Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/29687
Title: Central core disease due to recessive mutations in RYR1 gene: Is it more common than described?
Authors: Kossugue, Patricia M.
Paim, Julia F.
Navarro, Monica M.
Silva, Helga C.
Pavanello, Rita C. M.
Gurgel-Giannetti, Juliana
Zatz, Mayana
Vainzof, Mariz
Universidade de São Paulo (USP)
Sarah Network Rehabil Hosp
Universidade Federal de São Paulo (UNIFESP)
Universidade Federal de Minas Gerais (UFMG)
Keywords: central core disease
congenital myopathy
malignant hyperthermia
ryanodine receptor
RYR1
Issue Date: 1-May-2007
Publisher: Wiley-Blackwell
Citation: Muscle & Nerve. Hoboken: John Wiley & Sons Inc, v. 35, n. 5, p. 670-674, 2007.
Abstract: Central core disease (CCD) is an autosomal-dominant congenital myopathy, with muscle weakness and malignant hyperthermia (MH) susceptibility. We identified two of nine Brazilian CCD families carrying two mutations in the RYR1 gene. the heterozygous parents were clinically asymptomatic, and patients were mildly affected, differing from the few autosomal-recessive cases described previously. Recessive inheritance in CCD may therefore be more common than previously appreciated, which has important implications for genetic counseling and MH prevention in affected families.
URI: http://repositorio.unifesp.br/handle/11600/29687
ISSN: 0148-639X
Other Identifiers: http://dx.doi.org/10.1002/mus.20715
Appears in Collections:Em verificação - Geral

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