Myotonia dystrophic
Myotonia dystrophic is a hereditary disease characterized by a combination of myopathy and myotonia.
Etiology, pathogenesis. A systemic anomaly of lipid membrane elements is assumed.
Symptoms, course. The first manifestation of the disease is myotonia, which occurs between 15 and 40 years. Then, atrophy of the muscles of the face, neck and distal parts of the extremities is added. Muscular defects are usually accompanied by heart damage, cataracts, hypogonadism, frontal baldness, respiratory insufficiency. The disease lasts for years, slowly disabling patients. The cause of death is heart attack or pneumonia.
Treatment. Means that mitigate myotonia, and symptomatic measures.
- 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
- Mononeuropathies
- Mucopolysaccharidosis
- Narcolepsy
- Neuralgia of the trigeminal nerve
- Neuropathy of the facial nerve
- Neuroreumatism
- Neurosyphilis
- Fainting
- Tearing deprive
- Tumors of the brain
- Tumors of the spinal cord
- Ophthalmoplegia
- Parkinsonism
- Perinatal encephalopathy
- Periodic family paralysis
- Peroneal amyotrophy Charcot-Marie
- 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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