Occurrence of Synpolydactyly and Omphalocele in a Fetus with a HOXD13 Mutation
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Synpolydactyly (SPD) is an autosomal dominant congenital limb disorder due to mutations in HOXD13 . It is a phenotypically heterogeneous condition characterized by syndactyly of the third finger (F3), fourth finger (F4) and/or fourth toe (T4), and fifth toe (T... ...
