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The diagnosis of Charcot neuroarthropathy is made clinically and should be considered whenever a patient presents with warmth and swelling around a joint in the presence of neuropathy. Although counterintuitive, pain is present in many cases despite the neuropathy.
Charcot–Marie–Tooth disease (CMT) is a hereditary motor and sensory neuropathy of the peripheral nervous system characterized by progressive loss of muscle tissue and touch sensation across various parts of the body.
Charcot–Marie–Tooth disease, an inherited demyelinating disease of the peripheral nervous system Neuropathic arthropathy , progressive degeneration of a weight bearing joint, also known as Charcot joint disease or Charcot arthropathy
Charcot-Marie-Tooth disease is an inherited, genetic condition. It occurs when there are mutations in the genes that affect the nerves in your feet, legs, hands and arms.
Jean-Martin Charcot (French: [ʒɑ̃ maʁtɛ̃ ʃaʁko]; 29 November 1825 – 16 August 1893) was a French neurologist and professor of anatomical pathology. [2] He worked on groundbreaking work about hypnosis and hysteria, in particular with his hysteria patient Louise Augustine Gleizes. [3]
Charcot's neurologic triad of symptoms of multiple sclerosis; Some anterolateral central arteries in the brain are known as Charcot's artery; Neuropathic arthropathy, Charcot's joint or Charcot foot; Amyotrophic lateral sclerosis, a motor neurone disease known as both Charcot's disease and Lou Gehrig's disease
In an exclusive clip, the talk show legend looks back on how easily he got prescription medication to manage his painful multiple sclerosis symptoms
Charcot's cholangitis triad: Right Upper Quadrant Pain, Fever, Jaundice: Ascending cholangitis: Charcot's neurologic triad: scanning speech, intention tremor, nystagmus: Multiple sclerosis: Triad of congenital toxoplasmosis: chorioretinitis, hydrocephalus, intracranial calcifications: Congenital toxoplasmosis: Triad of congenital rubella