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Myofibromatosis, infantile, 2

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Description

Infantile myofibromatosis is a disorder of mesenchymal proliferation characterized by the development of benign tumors in the skin, muscle, bone, and viscera. Soft tissue lesions may regress spontaneously. Visceral lesions are associated with high morbidity and mortality (summary by Martignetti et al., 2013). For a discussion of genetic heterogeneity of infantile myofibromatosis, see IMF1 (228550).

OMIM

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

11

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Genes

External Links

  • OMIM

    615293

  • Orphanet
  • HPO
  • Medgen

    C3809084

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