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Myopathy, myofibrillar, 9, with early respiratory failure

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Description

Hereditary myopathy with early respiratory failure (HMERF) is a slowly progressive myopathy that typically begins in the third to fifth decades of life. The usual presenting findings are gait disturbance relating to distal leg weakness or nocturnal respiratory symptoms due to respiratory muscle weakness. Weakness eventually generalizes and affects both proximal and distal muscles. Most affected individuals require walking aids within a few years of onset; some progress to wheelchair dependence and require nocturnal noninvasive ventilatory support about ten years after onset. The phenotype varies even among individuals within the same family: some remain ambulant until their 70s whereas others may require ventilator support in their 40s.

GeneReviews

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

2,233

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Genes

External Links

  • OMIM

    603689

  • Orphanet

    178464

  • HPO
  • Medgen

    C1863599

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