Cranial neural crest cells (NCCs) are the origin of the anterior part of the face and the head.
Cranial NCCs are multipotent cells giving rise to bones, cartilage, adipose-tissues in the …

Analyzed endometrial cancer (EC) genomes have allowed for the identification of molecular
signatures, which enable the classification, and sometimes prognostication, of these …

Objective: This retrospective study aims to evaluate the utility of exome sequencing (ES) in
identifying genetic causes of congenital orofacial clefts (OFCs) in fetuses with or without …

Background Craniosynostosis (CS), premature fusion of one or more cranial sutures, leads
to abnormal skull development, impacting both facial esthetics and oral function. This study …

Objective Apert syndrome (AS) is a rare congenital craniofacial disorder that requires a
multidisciplinary approach to treatment and multiple surgeries. Given that cleft palate (CP) is …

The purpose of this research is to investigate variability in emotional expression that exists
across different types of emotion, including different ages and gender of adolescents with …

Introducción: El Síndrome de Apert es una patología poco común, posee una prevalencia
mundial de 1 por cada 65 a 160 mil nacidos vivos, a su vez presenta un patron de herencia …

El síndrome de Apert, también llamado acrocefalosindactilia tipo 1, se caracteriza por el
cierre precoz de las suturas craneales (craneosinostosis), sindactilia simétrica de pies y …