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Fatal infantile hypertonic myofibrillar myopathy

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Description

Fatal infantile hypertonic myofibrillar myopathy is a severe autosomal recessive muscular dystrophy with onset in the first weeks of life after a normal neonatal period. Affected infants show rapidly progressive muscular rigidity of the trunk and limbs associated with increasing respiratory difficulty resulting in death before age 3 years (summary by Del Bigio et al., 2011).

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

15

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Genes

External Links

  • OMIM

    613869

  • Orphanet

    280553

  • HPO
  • Medgen

    C3151236

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