Craniosynostosis is a common cranial malformation occurring in 1 per 2,000–2,500 births. Isolated defects (nonsyndromic) occur in ~75% of cases and are thought to have multifactorial etiology.

Craniosynostosis is a rare condition in which an infant has an abnormally shaped skull after the cranial ... Familial incidence and associated symptoms in a population of individuals with ...

Craniosynostosis is the early fusion of the cranial sutures, which poses numerous diagnostic and medical complications. It is a frequent abnormality that affects 3–5 out of every 10,000 babies.

The familial cases of craniosynostosis syndromes are quite rare but provide a way of mapping genes that are involved in the pathogenesis of craniosynostosis and in the development of the skull.

Craniosynostosis is a birth defect that can cause problems with a baby's head shape and later ... Genetic tests and other physical features usually help the doctor identify the syndromes that ...

(Medical Xpress)—Researchers at the University of Oxford have discovered two new genetic causes of craniosynostosis, a rare bone condition that can inhibit brain growth in children.

Metopic craniosynostosis is a rare condition in infants in which the metopic suture, a part of the skull, ... However, it may result from both genetic and environmental factors.

Scientists have identified two genetic risk factors for the most common form of non-syndromic craniosynostosis, a birth defect in which the bony plates of an infant's skull prematurely fuse.

An international team of geneticists, pediatricians, surgeons and epidemiologists from 23 institutions across three continents has identified two areas of the human genome associated with the most ...

Learn all about Apert Syndrome, its causes, symptoms, diagnosis methods, and treatment options to manage this rare genetic disorder effectively. Read more ...