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  2. Ataxic cerebral palsy - Wikipedia

    en.wikipedia.org/wiki/Ataxic_cerebral_palsy

    Ataxic cerebral palsy is known to decrease muscle tone. [3] The most common manifestation of ataxic cerebral palsy is intention (action) tremor, which is especially apparent when carrying out precise movements, such as tying shoe laces or writing with a pencil. This symptom gets progressively worse as the movement persists, causing the hand to ...

  3. Cerebral palsy - Wikipedia

    en.wikipedia.org/wiki/Cerebral_palsy

    Ataxic cerebral palsy is known to decrease muscle tone. [116] The most common manifestation of ataxic cerebral palsy is intention (action) tremor, which is especially apparent when carrying out precise movements, such as tying shoe laces or writing with a pencil. This symptom gets progressively worse as the movement persists, making the hand shake.

  4. Autosomal recessive spastic ataxia of Charlevoix-Saguenay

    en.wikipedia.org/wiki/Autosomal_recessive...

    ARSACS is usually diagnosed in early childhood, approximately 12–24 months of age when a child begins to take their first steps. At this time, it manifests as a lack of coordination and balance resulting in frequent falls. Some of the signs and symptoms include: [5] stiffness of the legs; appendicular and trunk ataxia; hollow foot and hand ...

  5. Ataxia–telangiectasia - Wikipedia

    en.wikipedia.org/wiki/Ataxia–telangiectasia

    Cerebral palsy; Friedreich's ataxia; Cogan oculomotor apraxia; Each of these can be distinguished from A–T by the neurologic exam and clinical history. [citation needed] Cerebral palsy (CP) describes a non-progressive disorder of motor function stemming from malformation or early damage to the brain. CP can manifest in many ways, given the ...

  6. Autosomal dominant cerebellar ataxia, deafness, and narcolepsy

    en.wikipedia.org/wiki/Autosomal_dominant...

    This condition was first discovered in 1995 by Melberg et al. when they described 5 members of a 4-generation Swedish family where cerebellar ataxia and sensorineural deafness presented as an autosomal dominant trait, 4 of them had narcolepsy and 2 had diabetes mellitus. The oldest members had psychiatric symptoms, neurological anomalies, and ...

  7. Spinocerebellar ataxia type 1 - Wikipedia

    en.wikipedia.org/wiki/Spinocerebellar_ataxia_type_1

    Many ataxic disorders which were historically identified as Marie's ataxia, olivopontocerebellar atrophy or other names were now reclassified as types of spinocerebellar ataxia, each type numbered in order as a new locus was found. [76] In 1993, the gene and a mutation causing spinocerebellar ataxia type 1 was identified.

  8. Management of cerebral palsy - Wikipedia

    en.wikipedia.org/wiki/Management_of_cerebral_palsy

    Function gait training in children and young adults with cerebral palsy improves their ability to walk. [18] There is evidence that antigravity treadmill training may improve the gait and balance of those children with diplegic cerebral palsy, it may also reduce risk of falls in these children. [19] [non-primary source needed]

  9. Autosomal dominant cerebellar ataxia - Wikipedia

    en.wikipedia.org/wiki/Autosomal_dominant...

    In terms of the genetics of autosomal dominant cerebellar ataxia 11 of 18 known genes are caused by repeated expansions in corresponding proteins, sharing the same mutational mechanism. SCAs can be caused by conventional mutations or large rearrangements in genes that make glutamate and calcium signaling, channel function, tau regulation and ...