enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  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. 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 ...

  4. 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.

  5. 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. ... There are some treatments to help people manage Charcot-Marie-Tooth disease, such as physical therapy and occupational therapy.

  6. Alan Jackson announces his farewell tour after more than a ...

    www.aol.com/lifestyle/alan-jackson-announces...

    Charcot-Marie-Tooth disease is a genetic neurological condition that causes damage to the peripheral nerves that connect the spine and brain to the arms and legs, according to the Mayo Clinic ...

  7. 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. [11] PMP22 encodes a 22-kD protein that comprises 2 to 5% of peripheral nervous system myelin. [12]

  8. Sarepta Therapeutics (SRPT) Q4 2024 Earnings Call Transcript

    www.aol.com/sarepta-therapeutics-srpt-q4-2024...

    Of note, for neurotrophin 3 or NT-3, we have optimized the construct for Charcot-Marie-Tooth type 1A or CMT1A using AAVrh74 and are now rapidly advancing to the clinic following exciting ...

  9. Polyneuropathy - Wikipedia

    en.wikipedia.org/wiki/Polyneuropathy

    According to Lopate, et al., methylprednisolone is a viable treatment for chronic inflammatory demyelinative polyneuropathy (which can also be treated with intravenous immunoglobulin). The authors also indicate that prednisone has greater adverse effects in such treatment, as opposed to intermittent (high-doses) of the aforementioned medication.