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  2. Neuropathic arthropathy - Wikipedia

    en.wikipedia.org/wiki/Neuropathic_arthropathy

    Neuropathic arthropathy (also known as Charcot neuroarthropathy or diabetic arthropathy) refers to a progressive fragmentation of bones and joints in the presence of neuropathy. [1] It can occur in any joint where denervation is present, although it most frequently presents in the foot and ankle. [2]

  3. Charcot–Marie–Tooth disease - Wikipedia

    en.wikipedia.org/wiki/Charcot–Marie–Tooth...

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

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

    en.wikipedia.org/wiki/X-linked_Charcot–Marie...

    X-linked Charcot–Marie–Tooth 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 ...

  5. 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.

  6. How to treat athlete’s foot - AOL

    www.aol.com/news/treat-athlete-foot-203742074.html

    Dr. Scholl’s Instant Cool Athlete’s Foot Treatment $ at CVS Pharmacy The spray, which has a 4.5-star average rating from over 3,110 reviews on Amazon, feels cooling as it goes on.

  7. 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 Charcot–Marie–Tooth disease type 3, is a hereditary neurological disorder characterized by damage to the peripheral nerves, demyelination, and resulting progressive muscle wasting and somatosensory loss.

  8. Charcot disease - Wikipedia

    en.wikipedia.org/wiki/Charcot_disease

    Charcot disease can refer to several diseases named for Jean-Martin Charcot, such as: Amyotrophic lateral sclerosis, a degenerative muscle disease also known as Charcot disease or Lou Gehrig's disease; Charcot–Marie–Tooth disease, an inherited demyelinating disease of the peripheral nervous system

  9. Hereditary motor and sensory neuropathy - Wikipedia

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

    Motor symptoms seem to be more predominant than sensory symptoms. [2] Symptoms of these disorders include: fatigue, pain, lack of balance, lack of feeling, lack of reflexes, and lack of sight and hearing, which result from muscle atrophy. Patients can also have high arched feet, hammer toes, foot drop, foot deformities, and scoliosis.