Contiguous Xp21 deletion involving Duchenne muscular dystrophy and McLeod neuroacanthocytosis syndrome results in rapidly progressive and fatal cardiomyopathy

    Research output: Contribution to journalArticlepeer-review

    Original languageEnglish
    Pages (from-to)358-360
    Number of pages3
    JournalCardiology in the Young
    Volume35
    Issue number2
    DOIs
    StatePublished - Feb 2025

    ASJC Scopus Subject Areas

    • Pediatrics, Perinatology, and Child Health
    • Cardiology and Cardiovascular Medicine

    Keywords

    • DMD
    • Duchenne muscular dystrophy
    • McLeod neuroacanthocytosis syndrome
    • Xp21
    • cardiomyopathy
    • contiguous gene deletion syndrome
    • Chromosome Deletion
    • Neuroacanthocytosis/genetics
    • Humans
    • Male
    • Dystrophin/genetics
    • Disease Progression
    • Muscular Dystrophy, Duchenne/genetics
    • Amino Acid Transport Systems, Neutral
    • Fatal Outcome
    • Chromosomes, Human, X/genetics
    • Cardiomyopathy, Dilated/genetics
    • Cardiomyopathies/genetics

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