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Related Concept Videos

Disorders of the Skeletal Muscle01:28

Disorders of the Skeletal Muscle

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...
Alterations in Muscle Tone ll01:12

Alterations in Muscle Tone ll

Alterations in muscle tone are common manifestations of neurological disorders and reflect dysfunction within different nervous system regions. Spasticity, paratonia, and dystonia represent distinct forms of hypertonia, each with unique mechanisms, clinical features, and diagnostic importance.CharacteristicsSpasticity happens from upper motor neuron lesions and is characterized by velocity-dependent resistance to passive movement. Clinical features include:Exaggerated deep tendon reflexesClonus...
Satellite Stem Cells and Muscular Dystrophy01:21

Satellite Stem Cells and Muscular Dystrophy

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...
Alterations in Muscle Tone lll01:11

Alterations in Muscle Tone lll

Rigidity and myotonia are distinct abnormalities of muscle tone that affect resistance and relaxation during movement. Although both involve altered muscle contraction, they arise from different neurological and muscular mechanisms.CharacteristicsRigidity is characterized by uniform resistance to passive movement across the entire range, independent of speed, affecting flexors and extensors equally. It may appear as lead-pipe rigidity (smooth, constant resistance) or cogwheel rigidity...
Myasthenia Gravis: Diagnostic Tests01:15

Myasthenia Gravis: Diagnostic Tests

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...
Cross-bridge Cycle01:26

Cross-bridge Cycle

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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Related Experiment Video

Updated: Jun 27, 2026

Utility of Dissociated Intrinsic Hand Muscle Atrophy in the Diagnosis of Amyotrophic Lateral Sclerosis
08:16

Utility of Dissociated Intrinsic Hand Muscle Atrophy in the Diagnosis of Amyotrophic Lateral Sclerosis

Published on: March 4, 2014

Proximal muscle weakness in a 15-year-old boy.

Marcia V Felker1, Bhuwan P Garg

  • 1Department of Neurology, Division of Pediatric Neurology, Indiana University School of Medicine, Indianapolis, IN 46202, USA. mamccann@iupui.edu

Seminars in Pediatric Neurology
|December 17, 2008
PubMed
Summary

Proximal muscle weakness in children can stem from various conditions. This case highlights spinal muscular atrophy type III as a cause, distinct from typical myopathies.

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Tissue Triage and Freezing for Models of Skeletal Muscle Disease

Published on: July 15, 2014

Area of Science:

  • Neurology
  • Pediatrics
  • Genetics

Background:

  • Proximal muscle weakness is a common pediatric concern with a wide range of potential causes.
  • Myopathies are frequently considered in the differential diagnosis of muscle weakness in children.

Observation:

  • A case study involving an adolescent male presenting with proximal muscle weakness.
  • The patient exhibited a mildly elevated creatine kinase level, a common biomarker for muscle damage.

Findings:

  • The diagnostic workup revealed spinal muscular atrophy type III (SMA III).
  • This contrasts with the initial suspicion of a myopathic process.

Implications:

  • Emphasizes the importance of considering neuromuscular junction disorders beyond primary muscle diseases.
  • Highlights the need for comprehensive diagnostic approaches in pediatric proximal weakness.
  • Broadens the understanding of SMA III presentation in adolescents.