FGFR3 and Camptodactyly: More than 60 distinct types of syndromic camptodactyly have been described in the literature, and camptodactyly phenotype has been observed in carriers with chromosomal abnormalities or gene mutations, including dup(15)(q24q26.3), 22q11 deletion, del(11)(q24.1), microdeletion at 2p15-2p16.1, and the fibroblast growth factor receptor 3 gene (FGFR3) p.R621H mutation [4–9].