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Myofibrillar MYH2 Myopathy in a Filipino-Chinese Male with Neuropathy, Ataxia, Arrhythmia and Short Stature- A Case Report

Author

Listed:
  • Gianne Camille Zozobrado de Castro

    (Resident Physician , Department of Neuroscience and Behavioral Medicine, University of Santo Tomas Hospital, Philippines)

  • Raymond L Rosales

    (Professor of Neuroscience and Academic Researcher, Research Center of Health Sciences, Faculty of Medicine and Surgery, University of Santo Tomas, Philippines)

Abstract

Myofibrillar myopathy (MFM) is a neuromuscular disorder, usually with adult onset and an autosomal dominant inheritance pattern, that results in slowly progressive weakening of limb muscles [1]. MFM may lead to multisystem involvement (eye, peripheral nerve, and heart), and progressive cardiorespiratory complications are potentially lethal [1].

Suggested Citation

  • Gianne Camille Zozobrado de Castro & Raymond L Rosales, 2023. "Myofibrillar MYH2 Myopathy in a Filipino-Chinese Male with Neuropathy, Ataxia, Arrhythmia and Short Stature- A Case Report," Biomedical Journal of Scientific & Technical Research, Biomedical Research Network+, LLC, vol. 48(3), pages 39719-39722, February.
    • Handle: RePEc:abf:journl:v:48:y:2023:i:3:p:39719-39722
    DOI: 10.26717/BJSTR.2023.48.007653
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