Clinical and genetic findings of two cases with Apert syndrome
Bol. méd. Hosp. Infant. Méx; 76 (1), 2019
Abstract Background: Craniosynostosis is described as the premature fusion of cranial sutures that belongs to a group of alterations which produce an abnormal phenotype. Case report: Two unrelated female patients with clinical findings of Apert syndrome-characterized by acrocephaly, prominent frontal...