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Related Concept Videos

Cross-bridge Cycle01:26

Cross-bridge Cycle

117.6K
As muscle contracts, the overlap between the thin and thick filaments increases, decreasing the length of the sarcomere—the contractile unit of the muscle—using energy in the form of ATP. At the molecular level, this is a cyclic, multistep process that involves binding and hydrolysis of ATP, and movement of actin by myosin.
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Amyloid Fibrils03:03

Amyloid Fibrils

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Amyloid fibrils are aggregates of misfolded proteins.  Under most circumstances, misfolded proteins are either refolded by chaperone proteins or degraded by the proteasome. However, in the case of a mutation or a disease, these proteins can accumulate to form large clusters and often further assemble to form elongated fibers, called fibrils. 
Amyloid deposits were observed as early as 1639 in the liver and the spleen.   In 1854, Rudolph Virchow performed iodine staining,...
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Satellite Stem Cells and Muscular Dystrophy01:21

Satellite Stem Cells and Muscular Dystrophy

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Satellite stem cells or myosatellite cells are quiescent stem cells that Alexander Mauro first identified in 1961. These cells are located between the sarcolemma, the plasma membrane of muscle fibers, and the basal lamina, the connective tissue sheath covering it. These mononucleated cells are activated in response to muscle injury, can transform into myoblasts, and may form or repair muscle fibers. Myosatellite cells can provide additional myonuclei for muscle regeneration or return to a...
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Myasthenia Gravis: Diagnostic Tests01:15

Myasthenia Gravis: Diagnostic Tests

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Myasthenia gravis is an autoimmune condition affecting neuromuscular transmission, causing generalized weakness in skeletal muscles. Initial diagnoses rely on patients' signs, symptoms, and medical history. The challenge lies in distinguishing myasthenia from other muscular dystrophies. An important diagnostic feature is the significant improvement of symptoms after administering anticholinesterase inhibitors.
The edrophonium test is a diagnostic tool for myasthenia gravis. It involves...
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Myasthenia Gravis: Overview and Treatment01:20

Myasthenia Gravis: Overview and Treatment

1.5K
Myasthenia gravis is a neuromuscular transmission disorder characterized by weakness and increased fatigability of skeletal muscles. It is an autoimmune disease affecting approximately one in 2000 people, where antibodies against the α1 subunit of nicotinic acetylcholine receptors are produced.
These antibodies interfere with the function of the nicotinic receptors in three ways: by binding to the receptor and disrupting acetylcholine binding; by causing cross-linking of receptors which...
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Disorders of the Skeletal Muscle01:28

Disorders of the Skeletal Muscle

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The clinical conditions affecting the skeletal muscle tissue are broadly categorized as musculoskeletal and neuromuscular disorders.
Musculoskeletal disorders
Musculoskeletal disorders involve injuries and conditions affecting the skeletal muscles and associated connective tissues. These disorders can arise from acute biomechanical stresses or chronic overuse and can occur across different age groups. Common injuries include sprains, fractures, and muscular strains, often resulting from...
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Related Experiment Video

Updated: Jul 11, 2025

Tissue Triage and Freezing for Models of Skeletal Muscle Disease
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Tissue Triage and Freezing for Models of Skeletal Muscle Disease

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Tubular aggregate myopathy causing progressive fatiguable weakness.

Qihua Fan1, Kelly Gwathmey2, Xinli Du2

  • 1Neurology, Virginia Commonwealth University, Richmond, Virginia, USA qihua.fan@vcuhealth.org.

Practical Neurology
|November 3, 2023
PubMed
Summary
This summary is machine-generated.

Tubular aggregate myopathies are rare disorders. This case highlights a patient with this condition presenting with myasthenic syndrome, emphasizing muscle biopsy

Area of Science:

  • Neurology
  • Rare Diseases
  • Muscle Disorders

Background:

  • Tubular aggregate myopathies (TAMs) are rare neuromuscular disorders.
  • They present with diverse clinical features, sometimes mimicking myasthenic syndrome.
Keywords:
MUSCLE DISEASEMYASTHENIAMYOPATHYNEUROPATHOLOGY, MUSCLE

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  • Diagnostic challenges exist due to heterogeneous phenotypes.