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Arthrogryposis multiplex congenita 3, myogenic type

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Description

Myogenic-type arthrogryposis multiplex congenita-3 (AMC3) is an autosomal recessive disorder characterized by decreased fetal movements, hypotonia, variable skeletal defects, including clubfoot and scoliosis, and delayed motor milestones with difficulty walking (summary by Baumann et al., 2017).

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

42

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Genes

External Links

  • OMIM

    618484

  • Orphanet
  • HPO
  • Medgen

    C5193121

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