Cap Myopathy: History
Please note this is an old version of this entry, which may differ significantly from the current revision.

Cap myopathy is a disorder that primarily affects skeletal muscles, which are muscles that the body uses for movement. People with cap myopathy have muscle weakness (myopathy) and poor muscle tone (hypotonia) throughout the body, but they are most severely affected in the muscles of the face, neck, and limbs. The muscle weakness, which begins at birth or during childhood, can worsen over time.

  • genetic conditions

1. Introduction

Affected individuals may have feeding and swallowing difficulties in infancy. They typically have delayed development of motor skills such as sitting, crawling, standing, and walking. They may fall frequently, tire easily, and have difficulty running, climbing stairs, or jumping. In some cases, the muscles used for breathing are affected, and life-threatening breathing difficulties can occur.

People with cap myopathy may have a high arch in the roof of the mouth (high-arched palate), severely drooping eyelids (ptosis), and a long face. Some affected individuals develop an abnormally curved lower back (lordosis) or a spine that curves to the side (scoliosis).

The name cap myopathy comes from characteristic abnormal cap-like structures that can be seen in muscle cells when muscle tissue is viewed under a microscope. The severity of cap myopathy is related to the percentage of muscle cells that have these caps. Individuals in whom 70 to 75 percent of muscle cells have caps typically have severe breathing problems and may not survive childhood, while those in whom 10 to 30 percent of muscle cells have caps have milder symptoms and can live into adulthood.

2. Frequency

Cap myopathy is a rare disorder that has been identified in only a small number of individuals. Its exact prevalence is unknown.

3. Causes

Mutations in the ACTA1, TPM2, or TPM3 genes can cause cap myopathy. These genes provide instructions for producing proteins that play important roles in skeletal muscles.

The ACTA1 gene provides instructions for making a protein called skeletal alpha (α)-actin, which is part of the actin protein family. Actin proteins are important for cell movement and the tensing of muscle fibers (muscle contraction). Thin filaments made up of actin molecules and thick filaments made up of another protein called myosin are the primary components of muscle fibers and are important for muscle contraction. Attachment (binding) and release of the overlapping thick and thin filaments allows them to move relative to each other so that the muscles can contract. The mutation in the ACTA1 gene that causes cap myopathy results in an abnormal protein that may interfere with the proper assembly of thin filaments. The cap structures in muscle cells characteristic of this disorder are composed of disorganized thin filaments.

The TPM2 and TPM3 genes provide instructions for making proteins that are members of the tropomyosin protein family. Tropomyosin proteins regulate muscle contraction by attaching to actin and controlling its binding to myosin. The specific effects of TPM2 and TPM3 gene mutations are unclear, but researchers suggest they may interfere with normal actin-myosin binding between the thin and thick filaments, impairing muscle contraction and resulting in the muscle weakness that occurs in cap myopathy.

4. Inheritance

Cap myopathy is an autosomal dominant condition, which means one copy of the altered gene in each cell is sufficient to cause the disorder. Most cases are not inherited; they result from new mutations in the gene and occur in people with no history of the disorder in their family.

5. Other Names for This Condition

  • cap disease
  • congenital myopathy with caps

This entry is adapted from the peer-reviewed paper


  1. Clarke NF, Domazetovska A, Waddell L, Kornberg A, McLean C, North KN. Capdisease due to mutation of the beta-tropomyosin gene (TPM2). Neuromuscul Disord. 2009 May;19(5):348-51. doi: 10.1016/j.nmd.2009.03.003.
  2. De Paula AM, Franques J, Fernandez C, Monnier N, Lunardi J, Pellissier JF,Figarella-Branger D, Pouget J. A TPM3 mutation causing cap myopathy. Neuromuscul Disord. 2009 Oct;19(10):685-8. doi: 10.1016/j.nmd.2009.06.365.
  3. Goebel HH. Cap disease uncapped. Neuromuscul Disord. 2007 Jun;17(6):429-32.
  4. Hung RM, Yoon G, Hawkins CE, Halliday W, Biggar D, Vajsar J. Cap myopathycaused by a mutation of the skeletal alpha-actin gene ACTA1. Neuromuscul Disord. 2010 Apr;20(4):238-40. doi: 10.1016/ Neuromuscul Disord.2010 Aug;20(8):567.
  5. Lehtokari VL, Ceuterick-de Groote C, de Jonghe P, Marttila M, Laing NG, Pelin K, Wallgren-Pettersson C. Cap disease caused by heterozygous deletion of thebeta-tropomyosin gene TPM2. Neuromuscul Disord. 2007 Jun;17(6):433-42.
  6. Marttila M, Lemola E, Wallefeld W, Memo M, Donner K, Laing NG, Marston S,Grönholm M, Wallgren-Pettersson C. Abnormal actin binding of aberrantβ-tropomyosins is a molecular cause of muscle weakness in TPM2-related nemalineand cap myopathy. Biochem J. 2012 Feb 15;442(1):231-9. doi: 10.1042/BJ20111030.
  7. Ochala J. Thin filament proteins mutations associated with skeletalmyopathies: defective regulation of muscle contraction. J Mol Med (Berl). 2008Nov;86(11):1197-204. doi: 10.1007/s00109-008-0380-9.
  8. Ohlsson M, Quijano-Roy S, Darin N, Brochier G, Lacène E, Avila-Smirnow D,Fardeau M, Oldfors A, Tajsharghi H. New morphologic and genetic findings in capdisease associated with beta-tropomyosin (TPM2) mutations. Neurology. 2008 Dec2;71(23):1896-901. doi: 10.1212/01.wnl.0000336654.44814.b8.
  9. Waddell LB, Kreissl M, Kornberg A, Kennedy P, McLean C, Labarre-Vila A,Monnier N, North KN, Clarke NF. Evidence for a dominant negative diseasemechanism in cap myopathy due to TPM3. Neuromuscul Disord. 2010 Jul;20(7):464-6. doi: 10.1016/j.nmd.2010.05.012.
This entry is offline, you can click here to edit this entry!
Video Production Service