What pathology is called Weber's syndrome? Weber's syndrome: causes, signs and treatment

Sturge-Weber Syndrome - hereditarydisease belonging to a group of alternating syndromes. It combines the defeat of the cranial nerves from the side of the hearth and the disturbance of the sensory and motor functions on the opposite side. Weber's syndrome is called a neurologic syndrome, in which the spine or the nucleus of the oculomotor nerve is damaged. Characteristic manifestations of the disease are reflected on the face, on the side of the focus there is ptosis, mydriasis, strabismus, contralateral central hemiplegia, paralysis of the muscles of the face and tongue.

Weber's syndrome: signs

Weber's syndrome is a disease, whenwhich appear on the affected areas of the skin of the angioma, angiomas of the vessels of the eye, conjunctiva are also observed; possibly the development of cataracts, glaucoma, as well as detachment of the retina.

On the mild cervicalmultiple angiomas, which also spread to the face and adjacent tissues, show characteristic neurological symptoms. Most often the disease affects the area of the upper jaw and the ocular trigeminal nerve. Damages to the soft shell of the brain can be either only on one side, or affect both.

The affected area of the face is covered with specific spots of red, while in addition to the nervous system, the disease can affect the internal organs.

Weber's syndrome is characterized by the following manifestations:

In the images of MRI or CT, manifestations of leptomeningeal angioma.
Convulsive reactions.
Delay of mental development (idiocy, oligophrenia).
Increased intraocular pressure.
Deficiency of vision.
Hemiparesis.
Gemiatrophy.
Angiomas (the skin is covered with red vascular spots).

Varieties of Weber's syndrome

There are several main varieties. Above is the described disease - Weber's syndrome. The photo shows how a person suffering from this pathology looks. The disease is divided into:

Schirmer-syndrome - the development of early glaucoma with manifestations of cutaneous and ocular angioma.
Milles-syndrome - the development of the hemangioma of the eye without the addition of early glaucoma with manifestations of angioma on the skin and in the eye area.
Knud-Rrubbe-syndrome is a manifestation of angioma of the encephalotrigeminal.
Weber-Dumitri-syndrome - the manifestation of epilepsy, seizures, developmental lag, hemihypertrophy.
Jahnke-syndrome - angioma of the skin, areas of the brain.
Loford-syndrome - angioma of the eyeball without its increase.

Weber's syndrome: causes

The cause of the disease is thatduring the development of the fetus, two embryonic leaflets are damaged: ectoderm and mesoderm. The development of this disease in children is extremely sporadic. The disease is transmitted mainly by the dominant alleles, but there is also a recessive inheritance.

The disease can develop in the fetus if, during pregnancy, it has been negatively affected. These include:

Smoking during pregnancy, especially in the early stages.
Alcohol consumption.
Drug use.
Intoxication of a pregnant woman of different etiology.
Uncontrolled use of medicines.
Sexual infections acquired during pregnancy.
Intrauterine infections.
Metabolic disorders in the future mother (hypothyroidism).

Often, the development of the disease affects only heredity. Weber's syndrome can not be infected in everyday life.

Diagnosis of the disease

The disease is diagnosed by characteristicmanifestations. Part of the patient's face is subject to angiomatous changes, increased eye pressure with a possible increase in the eyeball, there are epileptic seizures. If there is a suspicion of Weber's syndrome, the diagnosis and treatment are carried out by several doctors: an ophthalmologist, a neurologist, an epileptologist, a dermatologist.

To clarify the diagnosis,X-ray examination. On the pictures you can see the calcification of the cerebral cortex. Computer tomography gives an even more complete picture of the affected areas. In pictures taken with MRI, you can identify the thinning of the cerebral cortex, degeneration and atrophy of white matter. Hardware diagnosis is also necessary to exclude other, no less dangerous, diseases: brain tumors, abscess of the soft tissues of the brain, cysts.

A huge role in setting the right diagnosisplays an electroencephalography, as it makes it possible to determine the activity of bioelectric impulses in the brain in order to diagnose epilepsy in time. Most people with Weber's syndrome have epileptic seizures. Also, measurements of eye pressure, visual acuity, ophthalmoscopy, AV scanning are performed for the purpose of ophthalmic treatment.

Treatment of Weber Syndrome

Weber's syndrome is currently effectivehas no treatment, and the therapy is aimed at arresting symptoms and improving the quality of life of a person. The patient is prescribed anticonvulsant therapy with the use of various drugs:

"Depakin".
"Carbamazepine".
"Keppra."
Topiramate.
Finlepsin.

Quite often the patient does not respond to treatmentepileptic seizures, then the treating doctor may be prescribed the use of several drugs. If the intensive therapy does not help, then according to the neurosurgeon's indications, surgical treatment can be prescribed.

Increased eye pressure (glaucoma) is treatedspecial drops that reduce the secretion of the eye fluid. These drugs include "Timolol", "Alfagan", "Azopt", "Dorzolamide." However, this conservative therapy can be extremely inefficient, and then the only option is surgical treatment: the patient is trabeckullectomy or trabeculotomy.

Consequences and complications

Weber's syndrome is quite a dangerous disease. In the event that the ongoing conservative or surgical treatment has not yielded results and the patient's condition has not improved, a rather unfavorable prognosis is given. Uncontrolled epileptic syndrome can lead to dementia, oligophrenia, loss of vision, and the risk of stroke increases.

Prevention of the development of the disease

Despite the fact that the disease is hereditary, preventive measures carried out by a pregnant woman will significantly reduce the risk of developing the disease. Such activities include:

Abandonment of bad habits (especially during pregnancy).
Maintaining a healthy and healthy lifestyle. Frequent walks in the open air, healthy sleep.
Correct fractional power. Increase in the diet of foods high in fiber. Do not eat semi-finished or fried foods.
Timely registration at the time of pregnancy and visiting a doctor at the appointed time.
Drug use only for the doctor's prescription.

Weber's syndrome is a rare and dangerous disease,which directly affects the quality of human life. Trust in doctors, timely diagnosis and the passage of a prescribed treatment can change life for the better. It is also important not to let the disease run its course and not to take medicine without prescribing a doctor.