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  • Thumbnail for Muscle atrophy
    muscle atrophy is usually a finding (sign or symptom) in a disease rather than being a disease by itself. However, some syndromes of muscular atrophy are...
    30 KB (3,515 words) - 14:51, 8 July 2024
  • Thumbnail for Spinal muscular atrophy
    Spinal muscular atrophy (SMA) is a rare neuromuscular disorder that results in the loss of motor neurons and progressive muscle wasting. It is usually...
    89 KB (9,953 words) - 10:33, 25 May 2024
  • Thumbnail for Spinal and bulbar muscular atrophy
    Spinal and bulbar muscular atrophy (SBMA), popularly known as Kennedy's disease, is a rare, adult-onset, X-linked recessive lower motor neuron disease...
    43 KB (4,927 words) - 01:14, 8 November 2023
  • Thumbnail for Atrophy
    are said to have trophic effects. A diminished muscular trophic condition is designated as atrophy. Atrophy is reduction in size of cell, organ or tissue...
    8 KB (886 words) - 16:52, 24 March 2024
  • Thumbnail for Spinal muscular atrophies
    Spinal muscular atrophies (SMAs) are a genetically and clinically heterogeneous group of rare debilitating disorders characterised by the degeneration...
    16 KB (600 words) - 09:47, 18 March 2024
  • Thumbnail for Distal spinal muscular atrophy type 1
    spinal muscular atrophy type 1 (DSMA1), also known as spinal muscular atrophy with respiratory distress type 1 (SMARD1), is a rare neuromuscular disorder involving...
    16 KB (1,543 words) - 01:22, 24 March 2024
  • Thumbnail for Progressive muscular atrophy
    Progressive muscular atrophy (PMA), also called Duchenne–Aran disease and Duchenne–Aran muscular atrophy, is a disorder characterised by the degeneration...
    11 KB (1,316 words) - 21:13, 17 September 2022
  • Thumbnail for Motor neuron diseases
    Motor neuron diseases (category Systemic atrophies primarily affecting the central nervous system)
    (PBP), pseudobulbar palsy, progressive muscular atrophy (PMA), primary lateral sclerosis (PLS), spinal muscular atrophy (SMA) and monomelic amyotrophy (MMA)...
    21 KB (2,137 words) - 22:21, 9 July 2024
  • Thumbnail for X-linked spinal muscular atrophy type 2
    spinal muscular atrophy type 2 (SMAX2, XLSMA), also known as arthrogryposis multiplex congenita X-linked type 1 (AMCX1), is a rare neurological disorder involving...
    15 KB (1,604 words) - 01:57, 27 December 2023
  • Thumbnail for Muscular dystrophy
    in other organs. Over 30 different disorders are classified as muscular dystrophies. Of those, Duchenne muscular dystrophy (DMD) accounts for approximately...
    30 KB (2,240 words) - 21:42, 13 July 2024
  • Thumbnail for Charcot–Marie–Tooth disease
    atteignant plus tard les mains" [On a particular form of progressive muscular atrophy, often familial, beginning with the feet and legs and later reaching...
    40 KB (4,422 words) - 20:23, 1 July 2024
  • Thumbnail for Spinal muscular atrophy with lower extremity predominance 2A
    Spinal muscular atrophy with lower extremity predominance 2A (SMALED2A) is a rare neuromuscular disorder characterised by muscle weakness predominantly...
    3 KB (167 words) - 18:38, 28 May 2024
  • Neuromuscular Disorders is a peer-reviewed medical journal that focuses on neuromuscular disease, including muscular dystrophy, spinal muscular atrophy, and myasthenia...
    1 KB (49 words) - 03:43, 27 April 2023
  • Thumbnail for Hirayama disease
    America and Europe. The disease (disorder) was first described by Keizo Hirayama in 1959 as "juvenile muscular atrophy of unilateral upper extremity"....
    19 KB (2,254 words) - 04:13, 8 July 2024
  • Thumbnail for Neuromuscular disease
    that may reveal muscular disorders include direct clinical observations. This usually starts with the observation of bulk, possible atrophy or loss of muscle...
    13 KB (1,105 words) - 12:46, 8 February 2024
  • Thumbnail for Spinal muscular atrophy with progressive myoclonic epilepsy
    Spinal muscular atrophy with progressive myoclonic epilepsy (SMA-PME), sometimes called Jankovic–Rivera syndrome, is a very rare neurodegenerative disease...
    7 KB (514 words) - 09:50, 18 March 2024
  • Thumbnail for Distal spinal muscular atrophy type 2
    muscular atrophy type 2 (DSMA2), also known as Jerash type distal hereditary motor neuropathy (HMNJ), is a very rare childhood-onset genetic disorder...
    3 KB (218 words) - 04:33, 23 April 2023
  • Thumbnail for Facioscapulohumeral muscular dystrophy
    Facioscapulohumeral muscular dystrophy (FSHD) is a type of muscular dystrophy, a group of heritable diseases that cause degeneration of muscle and progressive...
    174 KB (16,344 words) - 14:45, 13 July 2024
  • Thumbnail for Genetic disorder
    sickle cell disease, Tay–Sachs disease, Niemann–Pick disease, spinal muscular atrophy, and Roberts syndrome. Certain other phenotypes, such as wet versus...
    35 KB (3,579 words) - 09:44, 9 July 2024
  • Thumbnail for ALS
    ALS (redirect from Primary muscular atrophy)
    disorders such as multiple sclerosis, post-polio syndrome, multifocal motor neuropathy, CIDP, spinal muscular atrophy, and spinal and bulbar muscular...
    130 KB (14,011 words) - 01:09, 4 July 2024
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