Subencephaly

Podencephaly is a rare disorder characterized by the absence of the brain. This is a rare condition that can be caused by a variety of reasons, including genetic disorders, head injuries, or infections.

Subencephaly usually manifests as an absence of the brain, which may be completely or partially removed. This condition can be detected in the early stages of pregnancy, when the fetus has not yet fully developed its brain.

If subencephaly is not detected early in pregnancy, it can lead to serious consequences for the baby. These children may have developmental problems such as mental retardation, speech, hearing and vision problems.

Treatment for subencephaly depends on the cause of its occurrence. In some cases, surgery may be necessary to remove part of the brain or replace it with other tissue.

It is important to note that subencephaly is a rare condition and most cases have no known cause. However, if you suspect that your child may have subencephaly, it is recommended that you see a doctor for diagnosis and treatment.

Podencephaly (Greek “under + enkephalia, head”) is a disease in which a tumor of different etiology forms on the peduncle of the brain - non-tumor, vascular. Most often, this pathology develops in children aged 2 to 7 years. Pathological compression of the medulla oblongata leads to poor circulation, development of mental retardation and memory loss.

What is Podencephaly?

Podencephaly is a rare hereditary disorder in which the brain is underdeveloped due to an abnormal development of the nervous system. This may occur during fetal development or shortly after birth. The complex mechanisms of this disease and its relationship with the level of human mental development have not been studied and remain a subject for research.

With the concept of encephalography Encephalography - what is it? This is a method of studying the structure of brain tissue using ultrasound. This technique is used by neurologists and neurosurgeons, as well as pediatricians to determine hidden diseases

Some researchers believe that subencephaly can only be diagnosed through medical imaging, such as magnetic resonance imaging (MRI). However, many people with the condition may experience only minor symptoms, such as problems with eye movement or learning difficulties.

The causes of subencephaly are unknown, but research has shown that it is a genetic disease, and is predominantly inherited through the mother's line. Genetic mutations and negative factors, such as infections during pregnancy, could affect the development of the baby's brain.

Treatment for subencephaly includes drug therapy and treatment of associated conditions such as seizures. If subencephaly causes significant developmental problems, special training and intervention may be required. Some people may use disability as