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Article

Imaging alterations in skeletal muscle channelopathies: a study in 15 patients.

Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology - 1 Dec 2015

Maggi Lorenzo, Brugnoni Raffaella, Canioni Eleonora, Maccagnano Elio, Bernasconi Pia, Morandi Lucia

Abstract excerpt

Skeletal muscle channelopathies (SMC), including non dystrophic myotonias (NDM) and periodic paralyses (PP), are characterized by considerable clinical overlap and clinical features not always allow addressing molecular diagnosis. Muscle imaging has been shown to be useful for differential diagnosis in neuromuscular disorders, however it has been relatively poorly investigated in SMC. We studied 15 patients...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Paralyses, Familial Periodic

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Source

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Identifiers

PMID: 27199537
PMCID: PMC4859077

Genes

CLCN1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

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