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Lambert Eaton Syndrome
Lambert eaton syndrome
Overview
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Related in the Kosmos
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Rare diseases
Legg-perthes disease
Lamellar ichthyosis
Leukodystrophy, globoid cell
Malignant hyperthermia
Multiple system atrophy
Multiple sulfatase deficiency
Lipofuscinoses
Neurological disorders
Progressive sclerosing poliodystrophy
Luschka-Magendie foramina atresia
Hereditary sensory and autonomic neuropathies
Olfaction disorders
Encephalomyelitis
Neuromyotonia
Lipofuscinoses
Diseases and disorders
(56)
Leiomyoma
Lateral epicondylitis
Leukemic reticuloen- dotheliosis
Lipoid nephrosis
Letterer-Siwe disease
Letterer-Siwe disease
Late syphilis
Myasthenia gravis
Cervical dystonia
Muscular dystrophies
Paraneoplastic cerebellar degeneration
Glossopharyngeal nerve diseases
Hyperostosis, cortical, congenital
Myopathies
Postpoliomyelitis syndrome
Fukuyama type muscular dystrophy
Purpura, schoenlein-henoch
Type i complex regional pain syndrome
Enterocolitis, pseudomembranous
Physiologic nystagmus
Fetofetal transfusion
Histiocytosis non-langerhans-cell
Lancereaux- -Mathieu-Weil Spirochetosis
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Encephalitis, arbovirus
Thymoma
Phytanic acid storage disease
Morvan disease
Sciatic nerve dysfunction
Paraneoplastic encephalomyelitis
Early constraint defects
Neuromuscular junction disease
Intervertebral disk displacement
Limbic encephalitis
Rosenthal syndrome
Metatropic dwarfism
Galactosemias
Brachial plexus neuropathies
Ependymoma
Blepharospasm
Optic neuropathy, ischemic
Small cell lung cancer
Guillain Barre Syndrome
Temporal arteritis
Marinesco sjogren syndrome
Legg-perthes disease
Lamellar ichthyosis
Progressive sclerosing poliodystrophy
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Olfaction disorders
Encephalomyelitis
Malignant hyperthermia
Multiple system atrophy
Multiple sulfatase deficiency
Lipofuscinoses
more...
Neurology
(17)
Lack of strength
Adrenoleuk- odystrophy
Myoclonic Encephalopathy of infants
Ramsay Hunt syndrome type I
Opsoclonus
Opsoclonus
Polymyositis
Transverse myelitis
Acquired epileptiform aphasia
Electromyography
Myasthenia gravis
Cervical dystonia
Muscular dystrophies
Paraneoplastic cerebellar degeneration
Sciatic nerve dysfunction
Limbic encephalitis
Guillain Barre Syndrome
Temporal arteritis
more...
Genodermatoses
Leopard syndrome
Lamellar ichthyosis
Phytanic acid storage disease
Multiple sulfatase deficiency
Genetic disorders
(13)
Emery-Dreifuss Syndrome
Loken Senior syndrome
Leopard syndrome
Lamellar ichthyosis
Muscular dystrophies
Muscular dystrophies
Adrenoleuk- odystrophy
Hyperostosis, cortical, congenital
Fukuyama type muscular dystrophy
Luschka-Magendie foramina atresia
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Galactosemias
Multiple sulfatase deficiency
more...
Symptoms
(9)
Limited range of motion
Blurry
Choking
Difficulty chewing
Difficulty talking
Difficulty talking
Paralysis
Swallowing difficulty
Weakness
Lack of strength
more...
Medical tests
Muscle biopsy
Plasmapheresis
Lobectomy
Leiomyoma
Electromyography
Causes, incidence, and risk factors
Antibodies
Autoimmune disease
Carcinoma
Muscle contraction
Myasthenia gravis
Signs and tests
EMG
Muscle atrophy
Nerve conduction study
Edrophonium
Caption
Mitochondrion
Nicotinic acetylcholine receptor
Sarcolemma
Synaptic vesicle
See also
(20)
Lateral collateral ligament
Ovovegetarian
Leukemoid reaction
Lactovegetarian
Langhans giant cell
Langhans giant cell
Livedo reticularis
Lems
Neuromuscular junction
3,4-diaminopyridine
Botulinum toxin type a
Hirayama syndrome
Eisenmenger
Tensilon test
Acetylcholine receptor
Autoimmune diseases
Paraneoplastic syndromes
Paraneoplastic syndromes, nervous system
Immune system
Muscle
Intravenous immunoglobulin
more...
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