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  2. Charcot–Marie–Tooth disease - Wikipedia

    en.wikipedia.org/wiki/CharcotMarieTooth...

    CharcotMarieTooth disease; Other names: CharcotMarieTooth neuropathy, peroneal muscular atrophy, Dejerine-Sottas syndrome: The foot of a person with CharcotMarieTooth disease: The lack of muscle, a high arch, and claw toes are signs of this genetic disease.

  3. Neuropathic arthropathy - Wikipedia

    en.wikipedia.org/wiki/Neuropathic_arthropathy

    Diabetes is the foremost cause in America today for neuropathic joint disease, [5] and the foot is the most affected region. In those with foot deformity, approximately 60% are in the tarsometatarsal joints (medial joints affected more than lateral), 30% metatarsophalangeal joints, and 10% have ankle disease. Over half of diabetic patients with ...

  4. Hereditary neuropathy with liability to pressure palsy

    en.wikipedia.org/wiki/Hereditary_neuropathy_with...

    PMP22 point mutations, such as the frameshift mutation Gly94fsX222 (c.281_282insG), can cause clinical overlap between PNPP and CharcotMarieTooth disease type 1A. Missense, nonsense, and splice site mutations have been described. [10] PMP22 encodes a 22-kD protein that comprises 2 to 5% of peripheral nervous system myelin. [11]

  5. Hereditary motor and sensory neuropathy - Wikipedia

    en.wikipedia.org/wiki/Hereditary_motor_and...

    CharcotMarieTooth disease was first described in 1886 by Jean-Martin Charcot, Pierre Marie, and independently Howard Henry Tooth. [2] In the 1950s, further classification occurred and separated patients into two distinct groups. Group one was characterized by slow nerve conduction velocities and demyelinating neuropathy.

  6. Dejerine–Sottas disease - Wikipedia

    en.wikipedia.org/wiki/Dejerine–Sottas_disease

    Dejerine–Sottas disease, also known as, Dejerine–Sottas syndrome, [3] hereditary motor and sensory polyneuropathy type III, and CharcotMarieTooth disease type 3, is a hereditary neurological disorder characterized by damage to the peripheral nerves, demyelination, and resulting progressive muscle wasting and somatosensory loss.

  7. X-linked Charcot–Marie–Tooth disease - Wikipedia

    en.wikipedia.org/wiki/X-linked_CharcotMarie...

    X-linked CharcotMarieTooth disease type 5: This subtype is characterized by infancy/childhood-onset progressive distal limb muscle weakness and atrophy that affects both upper and lower extremities (although it is important noting that it appears and is more noticeable on the lower extremities), foot drop, gait abnormalities, bilateral ...

  8. What we know about Alan Jackson and Charcot-Marie-Tooth ... - AOL

    www.aol.com/news/know-alan-jackson-charcot-marie...

    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.

  9. Diabetic foot - Wikipedia

    en.wikipedia.org/wiki/Diabetic_foot

    Diabetic foot conditions can be acute or chronic complications of diabetes. [1] Presence of several characteristic diabetic foot pathologies such as infection, diabetic foot ulcer and neuropathic osteoarthropathy is called diabetic foot syndrome. The resulting bone deformity is known as Charcot foot.

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