16
Mar
Greig cephalopolysyndactyly syndrome and 7p14 deletion
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Greig cephalopolysyndactyly syndrome (GCPS) and chromosome 7p14 deletion facial dysmorphism and developmental delay. Greig cephalopolysyndactyly syndrome (GCPS) is an autosomal dominant disorder. The main manifestations of this condition are macrocephaly, facial dysmorphism and polysyndactyly (preaxial polydactyly is an association with syndactyly between several fingers and/or toes). Usually the genetic basis... Read More
