Learn more about Chiari malformation type 1, a rare brain condition that may be present in certain genes thanks to ...

Significant brain defects known as Chiari malformations could be down to the genes some of us have inherited from ...

According to new research, Neanderthal DNA genes could be the reason that some people are more prone to a type of headache-causing brain defect.

Chiari malformation type I (CMI) is a congenital neurological disorder characterized by the herniation of the cerebellar tonsils through the foramen magnum, which impairs cerebrospinal fluid ...

Objective A common symptom of Chiari I malformation (CIM) is headache, which is diagnosed using non-validated criteria from the International Headache Society (IHS). CIM-associated headaches should ...

Chiari-like malformation (CM) is a congenital disease characterized by a mismatch in size between the cranial vault of the skull that protects the brain and its contents. The disease is also ...

Chiari I Malformation (CM-I) is a disorder characterized by herniation of the cerebellar tonsils through the foramen magnum. The choice of the optimal surgical management of CM-I is still an open ...

Introduction Chiari I malformation (CM1) is an anatomical abnormality characterised by the cerebellar tonsils descending at least 5 mm below the foramen magnum. CM1 causes obstruction of cerebrospinal ...

The clinical efficacy study of treatment to Chiari malformation type I with syringomyelia under the minimally invasive surgery of resection of submeningeal cerebellar tonsillar herniation and ...