• Thumbnail for Charcot–Marie–Tooth disease
    CharcotMarieTooth disease (CMT) is a hereditary motor and sensory neuropathy of the peripheral nervous system characterized by progressive loss of muscle...
    40 KB (4,443 words) - 16:41, 14 March 2024
  • Classifications of CharcotMarieTooth disease refers to the types and subtypes of CharcotMarieTooth disease (CMT), a genetically and clinically heterogeneous...
    14 KB (276 words) - 01:02, 3 March 2024
  • Thumbnail for Jean-Martin Charcot
    hemorrhage. Charcot was among the first to describe CharcotMarieTooth disease (CMT). The announcement was made simultaneously with Pierre Marie of France...
    43 KB (4,658 words) - 11:59, 4 May 2024
  • Thumbnail for Dejerine–Sottas disease
    Dejerine–Sottas disease, also known as, Dejerine–Sottas syndrome, hereditary motor and sensory polyneuropathy type III, and CharcotMarieTooth disease type 3...
    8 KB (666 words) - 11:39, 12 November 2023
  • X-linked CharcotMarieTooth disease is a group of genetic disorders and a type of CharcotMarieTooth disease characterized by sensory loss associated...
    16 KB (1,756 words) - 11:03, 25 August 2023
  • Thumbnail for GJB1
    resulting in an inherited peripheral neuropathy called X-linked Charcot-Marie-Tooth Disease. Complications include the demyelination of oligodendrocytes...
    19 KB (2,339 words) - 00:53, 25 October 2023
  • disease also known as Charcot disease or Lou Gehrig's disease CharcotMarieTooth disease, an inherited demyelinating disease of the peripheral nervous...
    608 bytes (107 words) - 10:41, 15 December 2020
  • Thumbnail for SURF1
    with systemic cytochrome c oxidase (complex IV) deficiency, and Charcot-Marie-Tooth disease 4K (CMT4K). SURF1 is located on the q arm of chromosome 9 in...
    20 KB (2,402 words) - 07:22, 15 April 2024
  • Thumbnail for MFN2
    the onset/progression of different pathological conditions. Charcot-Marie-Tooth disease type 2A (CMT2A) is caused by mutations in the MFN2 gene. MFN2...
    28 KB (3,260 words) - 04:32, 4 January 2024
  • Thumbnail for Hereditary motor and sensory neuropathy
    was used mostly historically to denote the more common forms CharcotMarieTooth disease (CMT). With the identification of a wide number of genetically...
    9 KB (749 words) - 03:32, 18 February 2024
  • Thumbnail for Rheobase
    as a subsequent a decrease in the transmembrane Na+ gradient. CharcotMarieTooth disease (CMT) is the most common form of hereditary neuropathy and can...
    28 KB (3,516 words) - 10:35, 11 April 2024
  • syndrome Charcot d Charcot disease CharcotMarieTooth disease CharcotMarieTooth disease CharcotMarieTooth disease deafness dominant type CharcotMarie–Tooth...
    40 KB (3,648 words) - 19:46, 6 May 2024
  • Thumbnail for Pierre Marie
    the eponymous CharcotMarieTooth disease, being named along with Jean-Martin Charcot and Howard Henry Tooth (1856–1925). This disease is characterized...
    10 KB (1,080 words) - 20:37, 10 November 2023
  • Alzheimer's disease (AD) Ankylosing Spondylitis Amyotrophic lateral sclerosis (ALS, Lou Gehrig's disease) Cancers CharcotMarieTooth disease (CMT) Chronic...
    16 KB (1,614 words) - 16:12, 29 March 2024
  • Thumbnail for Hereditary neuropathy with liability to pressure palsy
    motor and sensory neuropathy (HMSN) disorders and is linked to CharcotMarieTooth disease (CMT). Symptoms and symptom onset vary; some individuals are...
    11 KB (1,115 words) - 15:50, 27 March 2024
  • Thumbnail for Somatic nervous system
    systemic. Charcot-Marie-Tooth disease, Myasthenia gravis, and Guillain-Barre syndrome are a few instances of them. The Charcot-Marie-Tooth (CMT) disease group...
    15 KB (1,704 words) - 13:57, 26 January 2024
  • Thumbnail for Pes cavus
    of any form of Charcot-Marie-Tooth disease at this time. The development of the cavus foot structure seen in Charcot-Marie-Tooth disease has been previously...
    15 KB (1,972 words) - 13:59, 2 November 2023
  • Autosomal dominant CharcotMarieTooth disease type 2 with giant axons is a rare subtype of hereditary motor and sensory neuropathy of the axons which...
    6 KB (558 words) - 07:32, 21 April 2023
  • Thumbnail for Polyneuropathy
    therefore as follows: Inherited - hereditary motor neuropathies, CharcotMarieTooth disease, and hereditary neuropathy with liability to pressure palsy Acquired...
    16 KB (1,471 words) - 04:51, 19 February 2024
  • describe any of the types of this disease which inhibit sensation. They are less common than Charcot-Marie-Tooth disease. Eight different clinical entities...
    29 KB (3,722 words) - 14:07, 11 April 2024
  • Thumbnail for Todd MacCulloch
    to a genetic neuromuscular disorder that affected his feet, Charcot-Marie-Tooth disease. After retiring from professional basketball, MacCulloch had...
    9 KB (797 words) - 00:19, 25 April 2024
  • Thumbnail for Myelin protein zero
    deficiency and are associated with neuropathies like CharcotMarieTooth disease and Dejerine–Sottas disease. In humans, the gene that encodes myelin protein...
    19 KB (2,227 words) - 09:52, 27 January 2024
  • Thumbnail for Foot drop
    amyotrophic lateral sclerosis, muscular dystrophy, poliomyelitis, CharcotMarieTooth disease, multiple sclerosis, cerebral palsy, hereditary spastic paraplegia...
    22 KB (2,681 words) - 17:24, 15 February 2024
  • Thumbnail for ALS
    ALS (redirect from Lou Gehrigs disease)
    referred to as Charcot's disease (not to be confused with CharcotMarieTooth disease or Charcot joint disease), because Jean-Martin Charcot was the first...
    130 KB (14,009 words) - 11:15, 19 April 2024
  • player, and his girlfriend Victoria Berezovich, an advocate for CharcotMarieTooth disease awareness; Natasha Urkow, a quadriplegic playwright and actress...
    2 KB (177 words) - 23:36, 28 September 2023
  • disorders: gene is extended in length "OMIM Entry - # 118220 - CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A; CMT1A". Rodan LH, Qi W, Ducker GS, Demirbas...
    42 KB (969 words) - 16:02, 3 April 2024
  • Thumbnail for Neurofilament light polypeptide
    high-sensitive single molecule array (SIMOA). It is associated with CharcotMarieTooth disease 1F and 2E. Neurofilament light polypeptide has been shown to...
    20 KB (2,153 words) - 10:03, 27 January 2024
  • Thumbnail for Schwann cell
    synaptic activity, and presentation of antigens to T-lymphocytes. CharcotMarieTooth disease, Guillain–Barré syndrome (acute inflammatory demyelinating polyradiculopathy...
    19 KB (2,448 words) - 13:51, 2 April 2024
  • R S T U V W X Y Z This list contains acronyms and initials related to diseases (infectious or non-infectious) and medical disorders. Acronyms in healthcare...
    28 KB (112 words) - 15:27, 5 May 2024
  • Thumbnail for Spinal muscular atrophy with lower extremity predominance 1
    gene (the gene responsible also for one of the axonal types of CharcotMarieTooth disease) and is inherited in an autosomal dominant manner. As with many...
    4 KB (339 words) - 09:49, 18 March 2024