and metopic craniosynostosis patients noted increased frequency of chronic cough. Our data suggest that the genetic component of nonsyndromic craniosynostosis appears to be suture specific.

the doctor may take a sample of the baby’s blood for genetic testing. The main treatment for craniosynostosis is surgery, usually within the first year of life. Surgery can help the skull to ...

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.

Genetic tests and other physical features usually help the doctor identify the syndromes that cause this condition. A small number of babies with mild craniosynostosis won’t need surgical treatment.

(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 ...

Craniosynostosis is a symptom of various genetic disorders, each of which has a distinct inheritance pattern and propensity for recurrence. It is essential that the family members of a child with ...