mirror-image polydactyly of hands & feet without other anomalies
Jump to navigation
Jump to search
Epidemiology
- very rare
Genetics
- most cases are sporadic
- rare parent-child transmissions, autosomal
- associated with translocation t(2;14)(p23.3;q13) involving MIPOL1
Clinical manifestations
- mirror-image duplication of digits
- occasionally associated with
- dimelia of the ulna & fibula
- tibial &/or fibular hypoplasia
- nasal abnormality
- other malformations