Oxycephaly is an anomaly of brain development in which its shape resembles that of an acute triangle. This is a rare congenital disorder characterized by the presence of three horns instead of two. Oxycephaly can be caused by genetic disorders, and may also have causes related to intrauterine development.
Clinically, oxycephaly manifests itself in the form of various symptoms, which depend on the severity of the disease. In severe cases of oxycephaly, the patient may experience problems with vision, hearing, speech, and motor coordination. In milder cases, oxycephaly may only manifest as headaches and dizziness.
Diagnosis of oxycephaly is based on MRI data of the brain. Treatment for oxycephaly depends on the severity of the disease and may include surgery, medication, and rehabilitation.
Oxycephaly is a rare disease that can lead to serious consequences for the health and life of the patient. Therefore, it is important to promptly identify oxycephaly and begin treatment to minimize possible complications.
In recent years, a form of unusual appearance called oxycephaly has been gaining popularity. Oxygenation is not a disease, it is simply an external change in the structure of the head. Do not confuse oxidation and skin abnormality. Oxic and atrophic forms of oxification have similar names due to the external similarity of skin defects in the form of stripes. But