Conditions / Genetic

multiple synostoses syndrome 4

info ยท Genetic

A multiple synostoses syndrome that is characterized by fusion of carpal and tarsal bones, as well as conductive hearing loss and that has_material_basis_in heterozygous mutation in the GDF6 gene on chromosome 8q22.

Signs and symptoms

  • Otosclerosis
  • Overlapping toe
  • Broad foot
  • Tarsal synostosis
  • Pes planus
  • Brachydactyly