OBJECTIVES: We describe the first cohort-based analysis of the impact of genetic disorders
in craniosynostosis. We aimed to refine the understanding of prognoses and pathogenesis …

BACKGROUND Craniosynostosis is a condition in which 2 or more of the skull bones fuse
prematurely. The spectrum of the disorder most commonly involves the closure of a single …

The meninges lie in the interface between the skull and brain, harboring lymphatic
vasculature and skull progenitor cells (SPCs). How the skull and brain communicate …

Craniosynostosis, the premature fusion of one or more cranial sutures of the skull, provides
a paradigm for investigating the interplay of genetic and environmental factors leading to …

The neural crest (NC) is a major contributor to the vertebrate craniofacial skeleton, detailed
in model organisms through embryological and genetic approaches, most notably in chick …

Craniosynostosis, or the premature fusion of one or more cranial sutures, is a relatively
common congenital defect that causes a number of morphologic and functional …

Craniosynostosis and supernumerary teeth most often occur as isolated developmental
anomalies, but they are also separately manifested in several malformation syndromes …

Phenotypic variation across mammals is extensive and reflects their ecological
diversification into a remarkable range of habitats on every continent and in every ocean …

In the previous few decades, all companies have produced data in large amounts from
different sources. It can be from business applications of their own, social media or other …

Carpenter syndrome is a pleiotropic disorder with autosomal recessive inheritance, the
cardinal features of which include craniosynostosis, polysyndactyly, obesity, and cardiac …