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