Charo-Marie's peroneal amyotrophy
Peroneal amyotrophy Charcot-Marie is a hereditary disease manifested by slowly progressing atrophy and weakness of the distal parts of the legs.
Etiology, pathogenesis. The reason is unknown. There is progressive degeneration of the peripheral nerves of the legs, and later of the hands, as well as the roots and anterior horns of the spinal cord.
Symptoms, course. The disease often begins in childhood and adolescence. The first signs are the atrophy of the peroneal muscles with the gradual development of the steppe (cockswalk). Atrophic paresis grows very slowly; In the later stages of the process, brushes are also involved. Tendon reflexes disappear. There is often pain and paresthesia in the legs, as well as light distal hypoesthesia. Coordinator sphere and pelvic functions do not suffer. The composition of the cerebrospinal fluid is normal. Electromyography and study of the speed of carrying out along the nerves testify to the neurogenic genesis of amyotrophy.
The diagnosis is not wasteful: polyneuropathies, even chronic ones, are formed much faster.
Treatment is symptomatic.
Forecast. Even after many years, patients usually retain the ability to move independently.
- Nervous diseases
- Epilepsy
- Spina Bifida
- Abscess of the brain
- Aneurysm of cerebral vessels
- Arachnoiditis
- Amyotrophic lateral sclerosis
- Hepatocerebral dystrophy
- Hydrocephalus
- Headache
- Dizziness
- Cerebral palsy
- Diencephalic (hypothalamic) syndrome
- Stroke stroke
- Coma
- Craniosteosis
- Leukodystrophy
- Meningitis
- Myasthenia gravis
- Migraine Neuralgia
- Migraine (hemicrania)
- Myelitis
- Myelopathy
- Microcephaly
- Myotonia inborn
- Myotonia dystrophic
- Mononeuropathies
- Mucopolysaccharidosis
- Narcolepsy
- Neuralgia of the trigeminal nerve
- Neuropathy of the facial nerve
- Neuroreumatism
- Neurosyphilis
- Fainting
- Tearing deprive
- Tumors of the brain
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- Ophthalmoplegia
- Parkinsonism
- Perinatal encephalopathy
- Periodic family paralysis
- Hepatic encephalopathy
- Flexopathy
- Polyneuropathies
- Poliomyelitis is an acute epidemic
- Poliradiculoneuropathy acute demyelinating Guillena-Baree
- Post-Puncture Syndrome
- Progressive muscular dystrophy
- Radiculopathies discogenic
- Multiple sclerosis
- Syringomyelia
- Spinal amyotrophy
- Tremor
- Fakomatosis
- Funicular myelosis
- Chorea
- Craniocerebral trauma
- Eidi Syndrome
- Encephalitis virus
- Epiduritis acute spinal
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