Developmental Medicine & Child Neurology · 2005 · 18 citations · 4 references
MedicineGeneticsMolecular GeneticsHuman GeneticsMedical GeneticsNeuromuscular DisordersGenetic DisordersGenetic SyndromesMuscle DisordersMuscle PathologyMuscular DystrophyGene Amplification TestingGenetic TestingGenetic Testing For MyopathyIndex Case InvestigationMuscle Biopsy HistologyMuscle Biopsy InterpretationMutationSkeletal Myopathy
In children with a myopathy, muscle biopsy, together with the clinical presentation, can guide further investigations. The presence of centrally located nuclei suggests a myotubular myopathy, and gene testing may confirm this diagnosis. We describe a male child with a mild form of X-linked myotubular myopathy for which repeated muscle biopsy did not show the characteristic pattern of centrally located nuclei. Myotubular myopathy was not contemplated, therefore, until a maternally related relative was shown to have the disorder. Genetic testing showed that the index case carried the same mutation in his MTM1 gene as this relative.
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Genotype–phenotype correlations in X-linked myotubular myopathy
Meriel McEntagart, Gretchen Parsons, Anna Buj‐Bello et al. · Neuromuscular Disorders · 2002 · 154 citations