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.

Myotonia

Myotonia is a hereditary disease related to channelopathy (diseases associated with the pathology of ion channels). It is manifested by delayed muscle relaxation. Characteristic signs are myotonic discharges detected by needle EMG, and myotonic phenomena that are detected during clinical examination. Congenital form is accompanied by muscular hypertrophy, dystrophic form, on the contrary, is accompanied…

Myopathy

Myopathy are a group of diseases based on various disorders in the metabolism and structure of muscle tissue, leading to a decrease in the strength of the affected muscles and restriction of motor activity. Typical features of myopathy are: progressive muscle weakness, the development of muscle atrophy, a decrease in tendon reflexes and muscle tone.…

Myoclonic Epilepsy

Myoclonic epilepsy is a disease based on myoclonic epileptic paroxysms. Episodes of myoclonic seizures in patients are combined with generalized clonic-tonic seizures, absences. Concomitant neurological symptoms depend on the form of epilepsy. Diagnostics includes anamnesis collection, assessment of neurological and mental status, electroencephalography, genealogical analysis, biochemical studies, neuroimaging. Treatment is carried out with anticonvulsants, with…

Myositis of the Back Muscles

Myositis of the back muscles is an inflammatory process accompanied by pain syndrome and the formation of nodules in the thickness of muscle tissue. It proceeds acutely or chronically. It is manifested by muscle tension and pain, mainly occurring in the morning or after physical exertion. To clarify the diagnosis and determine the cause of…

Myositis

Myositis is an inflammatory process in skeletal muscles. It can affect any muscle. The most characteristic common symptom is local pain in the muscle (or muscles), which increases with movements and palpation. Over time, due to the protective tension of the muscles, there may be a limitation of the volume of movements in the joints.…

Microgyria

Microgyria is a rare form of cortical dysplasia, for which it is typical to reduce the size of the convolutions of the cerebral cortex (CC) with an increase in their total number. The disease occurs due to monogenic anomalies, intrauterine neuroinfections, and other congenital structural diseases of the central nervous system. Microgyria is manifested by…

Myelopathy

Myelopathy is a generalized concept used in neurology to designate spinal cord lesions of various etiologies, usually having a chronic course. Clinically, they can manifest as disorders of muscle strength and tone, various sensory disorders, pelvic organ dysfunction. The task of diagnostic search in myelopathy is to identify the causal disease. For this purpose, spine…

Myelitis

Myelitis is a common name for any inflammatory processes of the spinal cord. Symptoms directly depend on the level and degree of the lesion; most often it is pain (its irradiation), paralysis, pelvic dysfunction, sensitivity disorders, and others. Diagnosis of myelitis includes a neurological examination and evaluation of the parameters of cerebrospinal fluid taken for…

Migraine with Aura

Migraine with aura is a paroxysmal primary cephalgia, before the appearance of which visual disturbances, disorders of the sensitive sphere or speech are observed. It differs from a simple migraine that occurs 10-60 minutes before the headache and disappears before its appearance with bright dots, lightning, dark or light spots in the eyes, distortion of…

Migraine

Migraine is the primary episodic form of headache, manifested by intense, paroxysmal headaches (more often unilateral) with a combination of neurological, vegetative and gastrointestinal manifestations. It usually appears for the first time at the age of 12 to 22 years. It ranks second in frequency after tension headache. Often a migraine attack occurs after some…