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Limb girdle and facial weakness in female carriers of X-linked myotubular myopathy mutations

  • Ian Sutton
  • , John Winer
  • , Andrew Norman
  • , S Liediti-Gallati
  • , F McDonald

Research output: Contribution to journalArticle

27 Citations (Scopus)

Abstract

Although X-linked myotubular myopathy (XLMTM) is a recessive disorder, heterozygous female carriers of MTM1 mutations may present with limb girdle and facial weakness. It is proposed that manifesting heterozygote females with XLMTM have a skewed pattern of X-chromosome inactivation. However, skewed X-chromosome inactivation was not detected in either the lymphocyte or muscle DNA of a woman who presented with limb girdle/facial weakness and was found to be heterozygous for the R224X mutation.
Original languageEnglish
Pages (from-to)900-902
Number of pages3
JournalNeurology
Volume57
Publication statusPublished - 1 Jan 2001

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