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  2. Spinal muscular atrophy - Wikipedia

    en.wikipedia.org/wiki/Spinal_muscular_atrophy

    Spinal muscular atrophy (SMA) is a rare neuromuscular disorder that results in the loss of motor neurons and progressive muscle wasting. [ 3 ] [ 4 ] [ 5 ] It is usually diagnosed in infancy or early childhood and if left untreated it is the most common genetic cause of infant death. [ 6 ]

  3. Spinal muscular atrophies - Wikipedia

    en.wikipedia.org/wiki/Spinal_muscular_atrophies

    Spinal muscular atrophies (SMAs) are a genetically and clinically heterogeneous group of rare debilitating disorders characterised by the degeneration of lower motor neurons (neuronal cells situated in the anterior horn of the spinal cord) and subsequent atrophy (wasting) of various muscle groups in the body. [1]

  4. Reducing daily sitting time by 40 minutes may help prevent ...

    www.aol.com/reducing-daily-sitting-time-40...

    Fat in the paraspinal muscles and insulin resistance are both related to back pain. The study was a secondary analysis of a randomized controlled trial. The trial involved 64 adults.

  5. Motor neuron diseases - Wikipedia

    en.wikipedia.org/wiki/Motor_neuron_diseases

    (D) Advanced thenar muscle atrophy. [8] Signs and symptoms depend on the specific disease, but motor neuron diseases typically manifest as a group of movement-related symptoms. [6] They come on slowly, and worsen over the course of more than three months. Various patterns of muscle weakness are seen, and muscle cramps and spasms may occur.

  6. Progressive muscular atrophy - Wikipedia

    en.wikipedia.org/wiki/Progressive_muscular_atrophy

    The importance of correctly recognizing progressive muscular atrophy as opposed to ALS is important for several reasons. The prognosis is a little better. A recent study found the 5-year survival rate in PMA to be 33% (vs 20% in ALS) and the 10-year survival rate to be 12% (vs 6% in ALS).

  7. Facioscapulohumeral muscular dystrophy - Wikipedia

    en.wikipedia.org/wiki/Facioscapulohumeral...

    Person with muscular dystrophy depicted by Duchenne. Based on the muscles involved, this person could have had FSHD. 1884: Landouzy and Dejerine describe a form of childhood progressive muscle atrophy with a characteristic involvement of facial muscles and distinct from pseudohypertrophic (Duchenne's MD) and spinal muscle atrophy in adults. [128]

  8. Jokela type spinal muscular atrophy - Wikipedia

    en.wikipedia.org/wiki/Jokela_type_spinal...

    The first symptoms include muscle cramps and muscle twitches affecting the upper and lower limbs. They appear usually after age of 40. The disease is slowly progressive with adult onset and results in weakness and mild muscle atrophy. [1] [3] The disease does not affect life expectancy. [1]

  9. Spinal cord injury - Wikipedia

    en.wikipedia.org/wiki/Spinal_cord_injury

    Complications can include muscle atrophy, loss of voluntary motor control, spasticity, pressure sores, infections, and breathing problems. In the majority of cases the damage results from physical trauma such as car accidents , gunshot wounds , falls , or sports injuries , but it can also result from nontraumatic causes such as infection ...

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