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  2. Spinocerebellar ataxia - Wikipedia

    en.wikipedia.org/wiki/Spinocerebellar_ataxia

    Spinocerebellar ataxia (SCA) is a progressive, degenerative, [1] genetic disease with multiple types, each of which could be considered a neurological condition in its own right.

  3. Congenital muscular dystrophy - Wikipedia

    en.wikipedia.org/wiki/Congenital_muscular_dystrophy

    [12] [15] Patients display muscle weakness and cerebellar and ocular malformations, with a life expectancy of less than 1 year. [ 9 ] [ 15 ] An additional dystroglycanopathy phenotype is Fukuyama congenital muscular dystrophy (FCMD) caused by a mutation in the Fukutin (FKTN) gene, which is the second most common type of muscular dystrophy in ...

  4. LAMA2 related congenital muscular dystrophy - Wikipedia

    en.wikipedia.org/wiki/LAMA2_related_congenital...

    [1] [2] For consensus, generally, the term congenital muscular dystrophy refers to a diverse group of childhood onset muscle diseases -usually occurring the first two years of life- and mostly inherited through an autosomal recessive mode. Congenital muscular dystrophies have known phenotype-genotype profiles and produce muscle degenerative ...

  5. Scoliosis - Wikipedia

    en.wikipedia.org/wiki/Scoliosis

    Scoliosis (pl.: scolioses) is a condition in which a person's spine has an irregular curve [2] in the coronal plane. The curve is usually S- or C-shaped over three dimensions. [2] [7] In some, the degree of curve is stable, while in others, it increases over time. [3]

  6. Spinal muscular atrophy - Wikipedia

    en.wikipedia.org/wiki/Spinal_muscular_atrophy

    In untreated SMA type II, the course of the disease is slower to progress and life expectancy is less than the healthy population. Death before the age of 20 is frequent, although many people with SMA live to become parents and grandparents. SMA type III has normal or near-normal life expectancy if standards of care are followed.

  7. Alternating hemiplegia of childhood - Wikipedia

    en.wikipedia.org/wiki/Alternating_hemiplegia_of...

    Symptoms usually manifest in the first 3 months of the child's life, with an average onset of 2.5 months. Frequently, some of these symptoms will manifest in the neonatal period. These paroxysmal symptoms are often used to help diagnose AHC, since there is no simple test for it. [citation needed]

  8. U.S. life expectancy rose significantly last year, hitting ...

    www.aol.com/news/u-life-expectancy-rose...

    From 2019 to 2021, U.S. life expectancy dropped from 78.8 years to 7 6.4. Covid deaths fell significantly last year: Whereas Covid was the fourth leading cause of death in 2022, it was the 10th in ...

  9. Rigid spine syndrome - Wikipedia

    en.wikipedia.org/wiki/Rigid_spine_syndrome

    Rigid spine syndrome, also known as congenital muscular dystrophy with rigidity of the spine (CMARS), is a rare and often debilitating neuromuscular disorder. It is characterized by progressive muscle stiffness and rigidity, particularly in the spine, which can severely limit mobility and impact quality of life.

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