“…Craniofacial phenotypic changes associated with Jacobs syndrome include macrocephaly, hypertelorism, and dental abnormalities, 1,2 with a few cases of microcephaly also being reported. 2,3 Craniosynostosis, although not specifically reported alongside Jacobs syndrome, is present in 1 out of 2000 to 2500 live births, about 75% to 85% of which are nonsyndromic. 4,5 Nonsyndromic craniosynostoses are classified based on which suture is prematurely fused: scaphocephaly or dolichocephaly (sagittal suture), anterior plagiocephaly (single coronal suture), posterior plagiocephaly (single lambdoid suture), trigonocephaly (metopic suture), brachycephaly (bi-coronal sutures), and oxycephaly or turricephaly (all or most sutures).…”