Dysencephaly Splanchnocystic

Splanchnocystic dysencephaly: features of the disease

Splanchnocystic dysencephaly is a rare congenital disease that is characterized by impaired development of the brain and internal organs. The name of the disease comes from the Greek words "dis-" (not) and "enkephalos" (brain), as well as "splanchnocystic" (relating to the internal organs).

The disease manifests itself in various forms, depending on which organs and systems it affects. Patients with splanchnocystic dysencephaly experience disturbances in brain development, which can lead to delayed psychomotor development, epilepsy, paralysis and other problems.

In addition, the disease can lead to deformation of internal organs such as the liver, lungs, heart and others, which can cause their dysfunction and lead to various complications.

Diagnosis of splanchnocystic dysencephaly is based on a clinical examination of the patient, as well as on the results of magnetic resonance imaging and other research methods.

Treatment of splanchnocystic dysencephaly is aimed at eliminating the symptoms of the disease and maintaining the functions of organs and systems of the body. Moreover, each case of the disease requires an individual approach and may require complex treatment, including drug therapy, physiotherapy, rehabilitation measures and other methods.

Thus, splanchnocystic dysencephaly is a rare and serious disease that requires a careful and comprehensive approach to treatment. Regular examination and consultation with specialists will help to promptly identify and effectively treat this disease.

Dysencephalic edema is a pathological condition characterized by the accumulation of serous fluid in the cavities and spaces of the skull.

The outer covering of the cerebral hemispheres is formed by a thin layer of dura mater. Embryologically, it originates from the xyphoid fold. Depending on individual characteristics