CAV3-related distal myopathy is one form of distal myopathy, a group of disorders characterized by weakness and loss of function affecting the muscles farthest from the center of the body (distal muscles), such as those of the hands and feet. People with CAV3-related distal myopathy experience wasting (atrophy) and weakness of the small muscles in the hands and feet that generally become noticeable in adulthood. A bump or other sudden impact on the muscles, especially those in the forearms, may cause them to exhibit repetitive tensing (percussion-induced rapid contraction). The rapid contractions can continue for up to 30 seconds and may be painful. Overgrowth (hypertrophy) of the calf muscles can also occur in CAV3-related distal myopathy. The muscles closer to the center of the body (proximal muscles) such as the thighs and upper arms are normal in this condition.

CAV3-related distal myopathy is part of a group of conditions called caveolinopathies, which are muscle disorders caused by mutations in the CAV3 gene. The CAV3 gene provides instructions for making a protein called caveolin-3, which is found in the membrane surrounding muscle cells. This protein is the main component of caveolae, which are small pouches in the muscle cell membrane. Within the caveolae, the caveolin-3 protein acts as a scaffold to organize other molecules that are important for cell signaling and maintenance of the cell structure.

CAV3 gene mutations result in a shortage of caveolin-3 protein in the muscle cell membrane and a reduction in the number of caveolae. Researchers suggest that a shortage of caveolae impairs the structural integrity of muscle cells, interferes with cell signaling, and causes the self-destruction of cells (apoptosis). The resulting degeneration of muscle tissue leads to the signs and symptoms of CAV3-related distal myopathy.

In addition to CAV3-related distal myopathy, CAV3 gene mutations can cause other caveolinopathies including limb-girdle muscular dystrophy, rippling muscle disease, isolated hyperCKemia, and a heart disorder called hypertrophic cardiomyopathy. Several CAV3 gene mutations have been found to cause different caveolinopathies in different individuals. It is unclear why a single CAV3 gene mutation may cause different patterns of signs and symptoms, even within the same family.

Normal Function

The CAV3 gene provides instructions for making a protein called caveolin-3, which is found in the membrane surrounding muscle cells. This protein is the main component of caveolae, which are small pouches in the muscle cell membrane. Within the caveolae, the caveolin-3 protein acts as a scaffold to organize other molecules that are important for cell signaling and maintenance of the cell structure. These molecules include the proteins that make up sodium channels, which transport positively charged sodium atoms (sodium ions) into cells. Sodium channels play a key role in a cell's ability to generate and transmit electrical signals. In cardiac muscle, sodium channels are involved in maintaining the heart's normal rhythm. Caveolin-3 may also help regulate calcium levels in the muscle cell, which control muscle contraction and relaxation.

Health Conditions Related to Genetic Changes

CAV3-related distal myopathy

At least two CAV3 gene mutations have been identified in people with distal myopathy, a disorder characterized by weakness and loss of function mainly affecting the muscles farthest from the center of the body (distal muscles), such as those of the hands and feet. Mutations that cause CAV3-related distal myopathy result in a shortage of caveolin-3 protein in the muscle cell membrane and a reduction in the number of caveolae. Researchers suggest that a shortage of caveolae impairs the structural integrity of muscle cells, interferes with cell signaling, and causes the self-destruction of cells (apoptosis). The resulting breakdown of muscle tissue leads to the signs and symptoms of CAV3-related distal myopathy.

Isolated hyperCKemia

At least four CAV3 gene mutations have been identified in individuals with isolated hyperCKemia. People with this condition have elevated levels of an enzyme called creatine kinase in the blood. Creatine kinase is released into the blood when muscle cells are damaged; however, people with isolated hyperCKemia have no muscle weakness or other symptoms of muscle disease. CAV3 gene mutations that cause isolated hyperCKemia lead to a caveolin-3 shortage that likely damages muscle cells. Although the damage is not severe enough to cause noticeable symptoms, it may lead to the elevated blood levels of creatine kinase that characterize isolated hyperCKemia.

Rippling muscle disease

At least 12 CAV3 gene mutations have been identified in people with rippling muscle disease, a condition in which the muscles are unusually sensitive to movement or pressure (irritable). Affected individuals may have muscle cramps, stiffness, and muscles that appear to ripple when they are stretched.

CAV3 gene mutations that cause rippling muscle disease result in a shortage of caveolin-3 protein in the muscle cell membrane. Researchers suggest that reduced caveolin-3 levels may impair the control of calcium levels in muscle cells, leading to abnormal muscle contractions in response to stimulation.

Limb-girdle muscular dystrophy

MedlinePlus Genetics provides information about Limb-girdle muscular dystrophy

Romano-Ward syndrome

MedlinePlus Genetics provides information about Romano-Ward syndrome

Other disorders

CAV3 gene mutations also can cause hypertrophic cardiomyopathy. Hypertrophic cardiomyopathy is a thickening of the heart (cardiac) muscle that forces the heart to work harder to pump blood. This condition can lead to heart failure.

When caused by CAV3 gene mutations, hypertrophic cardiomyopathy as well as limb-girdle muscular dystrophy, isolated hyperCKemia, rippling muscle disease, and distal myopathy (all described above) are classified as caveolinopathies. Several CAV3 gene mutations have been found to cause different caveolinopathies in different individuals. It is unclear why a particular CAV3 gene mutation may cause different patterns of signs and symptoms, even within the same family.

Mutations in the CAV3 gene have also been identified in people with long QT syndrome, which is a heart condition that causes the cardiac muscle to take longer than usual to recharge between beats. The irregular heartbeats (arrhythmia) can lead to fainting (syncope) or cardiac arrest and sudden death. Researchers suggest that CAV3 gene mutations may disrupt ion transport through sodium channels located in the caveolae. A disruption in ion transport may alter the way the heart beats, leading to the abnormal heart rhythm characteristic of long QT syndrome.

Other Names for This Gene

• CAV3_HUMAN
• caveolin-3
• LGMD1C
• LQT9
• M-caveolin
• MGC126100
• MGC126101
• MGC126129
• VIP-21
• VIP21

Genomic Location

This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. In most cases, an affected person has one parent with CAV3-related distal myopathy or another caveolinopathy. Rare cases result from new mutations in the gene and occur in people with no history of caveolinopathies in their family.

The prevalence of CAV3-related distal myopathy is unknown. Only a few affected individuals have been described in the medical literature.