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Contractures, pterygia, and variable skeletal fusions syndrome 1B

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Description

Contractures, pterygia, and spondylocarpotarsal fusion syndrome-1B (CPSFS1B) is characterized by contractures of proximal and distal joints, pterygia involving the neck, elbows, fingers, and/or knees, and variable vertebral, carpal, and tarsal fusions. Inter- and intrafamilial variability has been observed (Cameron-Christie et al., 2018). An autosomal dominant form of contractures, pterygia, and spondylocarpotarsal fusion syndrome (CPSFS1A; 178110) is caused by heterozygous mutation in the MYH3 gene.

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

21

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Genes

External Links

  • OMIM

    618469

  • Orphanet
  • HPO
  • Medgen

    C5193114

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