Nervous diseases are diseases that develop as a result of damage to the brain and spinal cord, as well as peripheral nerve trunks and ganglia. Nervous diseases are the subject of study of a specialized field of medical knowledge – neurology. Since the nervous system is a complex apparatus that connects and regulates all organs and systems of the body, neurology closely interacts with other clinical disciplines such as cardiology, gastroenterology, gynecology, ophthalmology, endocrinology, orthopedics, traumatology, speech therapy, etc. The main specialist in the field of nervous diseases is a neurologist.
ND can be genetically determined (Rossolimo-Steinert-Kurschmann myotonia, Friedreich’s ataxia, Wilson’s disease, Pierre-Marie ataxia) or acquired. Congenital malformations of the nervous system (microcephaly, basilar impression, Kimberly anomaly, Chiari anomaly, platybasia, congenital hydrocephalus), in addition to hereditary factors, can lead to unfavorable conditions of intrauterine development of the fetus: hypoxia, radiation, infection (measles, rubella, syphilis, chlamydia, cytomegaly, HIV), toxic effects, the threat of spontaneous termination of pregnancy, eclampsia, Rh conflict, etc. Infectious or traumatic factors affecting the nervous system immediately after the birth of a child (purulent meningitis, asphyxia of a newborn, birth trauma, hemolytic disease) often lead to the development of such nervous diseases as cerebral palsy, childhood epilepsy, oligophrenia.

Acquired ND are often associated with infectious lesions of various parts of the nervous system. As a result of infection, meningitis, encephalitis, myelitis, brain abscess, arachnoiditis, multiple encephalomyelitis, ganglioneuritis and other diseases develop. A separate group consists of traumatic etiology: TBI, spinal cord injury, traumatic neuritis. ND that occur in old age are mainly caused by vascular changes (dyscirculatory encephalopathy, TIA, ischemic stroke, hemorrhagic stroke), less often by metabolic disorders (Parkinson’s disease). The incidence of oncological nervous diseases remains high. The limited space inside the skull or spinal canal leads to the fact that even benign tumors of this localization (astrocytoma, craniopharyngioma, ganglioneuroma) have a malignant course. In addition, the problematic nature of complete removal of CNS tumors causes their frequent recurrence.

Clinical manifestations directly depend on which part of the nervous system was involved in the pathological process. Thus, nervous diseases with brain damage can be accompanied by headache, dizziness, gait and coordination disorders, speech disorders, hearing and vision loss, paresis and paralysis of a central nature, changes in the psyche. Nervous diseases associated with spinal cord pathology are manifested by motor and sensory disorders below the lesion level. Diseases of the peripheral nervous system (trigeminal neuralgia, facial neuritis, intercostal neuralgia, cervical plexitis, polyneuropathies, radial nerve neuropathy, femoral nerve neuropathy, etc.) are characterized by pain syndrome, sensitivity disorders, muscular atrophy, motor disorders, vegetative and trophic changes in the innervation zone of the affected nerve.

The foundation of instrumental diagnostics traditionally consists of such studies as radiography of the spine, Echo-EG, EEG, REG, electromyography, in children of the 1st year of life – neurosonography. They are replaced by more accurate diagnostic methods: computed tomography, MRI, PET of the brain, ultrasound of the vessels of the head, duplex scanning. And, if REG and echoencephalography, as methods of diagnosing nervous diseases, gradually lose their significance, then EMG and EEG remain indispensable. They make it possible to identify functional changes occurring in many that are not diagnosed by neuroimaging methods. In some nervous diseases, diagnostic search requires lumbar puncture, stereotactic biopsy, puncture of the ventricles of the brain, and other diagnostic operations. Since the nervous system is closely interconnected with other organs and systems of the body, for a more accurate diagnosis of nervous diseases, a neurologist (a pediatric neurologist) often needs consultations from other specialists: an ophthalmologist, an endocrinologist, a cardiologist, an orthopedist, etc.

Treatment as a rule, includes a whole range of measures aimed not only at combating the cause of the disease and its etiopathogenetic mechanisms, but also at maximum recovery of the neurological deficit resulting from the disease. For this purpose, physiotherapy, physical therapy, mechanotherapy, reflexology, manual therapy are widely used in the treatment of nervous diseases. Treatment of aneurysms, tumors, intracerebral hematomas, abscesses and cysts of the brain requires surgical intervention. In some cases, surgical treatment is used for epilepsy and Parkinson’s disease. Brain surgeries and spinal cord interventions are performed by neurosurgeons. They carry out modern surgical treatment of nervous diseases with the help of minimally invasive microsurgical techniques and under the control of neuroimaging. Methods of functional neurosurgery have been developed that are successfully used for torsion dystonia, cerebral palsy, Huntington’s chorea and other nervous diseases accompanied by muscle tone disorders, tremor or hyperkinesis.
You can learn more about the causes, symptoms, methods of diagnosis and treatment of individual nervous diseases in the corresponding section of the Medical Directory of Diseases. The Medic Journal website also provides descriptions of the main hardware studies that help diagnose various nervous diseases.

Beriberi

Beriberi is a disease caused by insufficient inclusion of thiamine (vitamin B1) in metabolic processes. Most often occurs when there is a deficiency in the intake of B1 with food, a violation of absorption in the gastrointestinal tract. Clinically, beriberi is manifested by bilateral polyneuropathy, cachexia, and cardiovascular disorders. It is possible to develop acute…

Basilar Migraine

Basilar migraine is a special variant of migraine caused by transient pathological changes in the blood supply area of the basilar artery. A headache attack occurs after an aura, which includes dizziness, ataxia, sensory disorders, visual disturbances, hearing impairment. Diagnosis is carried out by methods of neurological examination, REG, ultrasound or MRI angiography, MRI or CT…

Basilar Impression

Basilar impression is an acquired or congenital indentation into the skull of the occipital bone in the area of the craniovertebral junction. The decrease in the volume of the cranium and cranial (towards the skull) displacement of the spine that occur during basilar impression are the cause of the development of hydrocephalus, cerebellar disorders, disorders…

Atypical Facial Pain

Atypical facial pain is a chronic pain in the face that does not meet the criteria of other cranial neuralgias, is not associated with somatic pathologies. According to modern diagnostic criteria, atypical pain should be observed daily for at least two hours a day for three months or longer. The diagnostic program involves consultation with…

Athetosis

Athetosis is a separate form of subcortical hyperkinesis characterized by involuntary slow movements in the distal extremities with a change in muscle tone. It can be an integral part of the clinic of perinatal, hypoxic, hereditary-degenerative brain lesions. Athetosis is diagnosed clinically, the underlying disease is clarified on the basis of a study of the…

Cerebral Atherosclerosis

Cerebral atherosclerosis is the process of formation of atherosclerotic plaques inside the cerebral vessels, resulting in disorders of the cerebral blood supply. It may have a subclinical course or manifest itself as dyscirculatory encephalopathy, TIA, stroke. The diagnosis uses REG, ultrasound, duplex scanning or MRI of cerebral vessels, as well as electroencephalography, CT and brain…

Friedreich’s Ataxia

Friedreich’s ataxia is a genetic disease associated with impaired transport of iron from mitochondria and occurs with a predominant lesion of cells of the central and peripheral nervous system, cardiomyocytes, beta cells of the pancreas, bone tissue cells and retina. Friedreich’s ataxia is diagnosed using MRI of the brain and spinal cord, neurophysiological studies, and…

Ataxic Cerebral Palsy

Ataxic cerebral palsy is a type of cerebral palsy that occurs when the cerebellum or the frontal-bridge-cerebellar pathway is affected. The risk of developing pathology increases with prematurity, the action of teratogenic factors, birth trauma. The atactic form of paralysis is manifested by muscular hypotension, ataxia, cerebellar dysarthria, as well as intellectual disabilities of varying…

Ataxia

Ataxia is a disorder of coordination of movements; a very common violation of motor skills. The strength in the limbs is slightly reduced or completely preserved. Movements become inaccurate, awkward, their continuity and sequence are upset, the balance in the standing and walking position is disturbed. Static ataxia is a violation of balance in a…

Astrocytoma

Astrocytoma is a primary intracerebral neuroepithelial (glial) tumor originating from stellate cells (astrocytes). Disease can have different degrees of malignancy. Its manifestations depend on the localization and are divided into general (weakness, loss of appetite, headaches) and focal (hemiparesis, hemihypesthesia, coordination disorders, hallucinations, speech disorders, behavior changes). Astrocytoma is diagnosed on the basis of clinical data,…