What is Bethlem myopathy?
Bethlem myopathy is a rare disease that affects the skeletal muscles and connective tissue. The disease is characterized by progressive muscle weakness and joint stiffness (contractures) in the fingers, wrists, elbows, and ankles.
How common is Bethlem myopathy?
Bethlem myopathyis a rare congenital muscular dystrophy disease. Please discuss with your doctor for further information.
What are the symptoms of Bethlem myopathy?
Bethlem myopathy mainly affects skeletal muscles, which are the muscles used for movement. People with this disease experience progressive muscle weakness and joint stiffness (contractures) in their fingers, wrists, elbows, and ankles. The features of Bethlem myopathy can appear at any age. In some cases, the symptoms start before birth with decreased fetal movements. In others, low muscle tone (hypotonia) and a stiff neck (torticollis) develop during infancy. During childhood, developmental delay may be noted. For example a baby with Bethlem myopahy may learn to sit by themselves or walk later than usual. In some, symptoms don’t occur until adulthood, when a person may notice muscle weakness. By the age of 50-years-old, approximately two-thirds (66%) of people with Bethlem myopathy will need to use a walker, cane, or wheelchair.
In addition to the muscle problems, some people with Bethlem myopathy have skin abnormalities. These abnormalities may include small bumps called follicular hyperkeratosis that develop around the elbows and knees or soft, velvety skin on the palms and soles. Some people may also have wounds that split open with little bleeding and widen over time to create shallow scars. Rarely, individuals with Bethlem myopathy may develop breathing problems as the disease progresses
The common symptoms of Bethlem myopathy are:
- Camptodactyly of finger
- EMG abnormality
- Joint stiffness
- Abnormality of the cardiovascular system
- Ankle contracture
- Autosomal dominant inheritance
- Autosomal recessive inheritance
- Congenital muscular torticollis
- Decreased fetal movement
- Distal muscle weakness
- Elbow flexion contracture
- Elevated serum creatine phosphokinase
- Limb-girdle muscle weakness
- Motor delay
- Neonatal hypotonia
- Proximal muscle weakness
- Respiratory insufficiency due to muscle weakness
- Skeletal muscle atrophy
- Slow progression
- Variable expressivity
There may be some symptoms not listed above. If you have any concerns about a symptom, please consult your doctor.
When should I see my doctor?
If you have any signs or symptoms listed above or have any questions, please consult with your doctor. Everyone’s body acts differently. It is always best to discuss with your doctor what is best for your situation.
What causes Bethlem myopathy?
Bethlem myopathy is caused by mutations (changes) in the COL6A1, COL6A2, or COL6A3 genes. These genes each provide instructions for making one component of a protein called type VI collagen. This protein plays an important role in the muscles, particularly skeletal muscles. Type VI collagen makes up part of the extracellular matrix, an intricate lattice that forms in the space between cells and provides structural support to the muscles.
Mutations in the type VI collagen genes result in the formation of abnormal type VI collagen or reduced amounts of type VI collagen. This decrease in amounts of normal type VI collagen disrupts the extracellular matrix surrounding muscle cells, which leads to the progressive muscle weakness and other signs and symptoms of Bethlem myopathy.
Bethlem myopathy is typically inherited in an autosomal dominant manner, meaning one copy of the altered gene in each cell is sufficient to cause the disease. We inherit one copy of each of our genes from our mother and the other from our father. Many cases of Bethlem myopathy result from new (de novo) mutations in the gene, meaning the mutations were not inherited from either parent. When people who have a new mutation in a gene causing Bethlem myopathy go on to have children, each of their children will have a 50% chance of inheriting the disease.
In some cases, a person who has Bethlem myopathy inherited the mutation from one affected parent. In these cases, future children of this parent will also have a 50% chance to inherit the disease. The parent who has the disease may be so mildly affected that they didn’t know they were showing symptoms of the disease at all.
In rare cases, Bethlem myopathy is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive disease each carry one copy of the mutated gene, but they typically do not show signs and symptoms of the disease. These individuals are known as carriers. When two carriers of a gene mutation causing Bethlem myopathy have children, for each child there is a:
- 25% chance that the child will have Bethlem myopathy
- 50% chance that the child will be a carrier of Bethlem myopathy like the parents
- 25% chance that the child will have two working copies of the gene that makes type VI collagen, so the child will not have Bethlem myopathy and will not be a carrier.
What increases my risk for Bethlem myopathy?
Please consult with your doctor for further information.
Diagnosis & treatment
The information provided is not a substitute for any medical advice. ALWAYS consult with your doctor for more information.
How is Bethlem myopathy diagnosed?
Bethlem myopathy is typically diagnosed based on a clinical evaluation that identifies signs and symptoms typical of people with the disease. A healthcare provider may recommend additional laboratory test including:
- Blood test measuring creatine kinase (CK) levels: these levels will typically be normal or only slightly elevated
- Skin biopsy
- Muscle MRI
- Electromyography (EMG)
Genetic testing of the COL6A1, COL6A2, and COL6A3 genes can confirm the diagnosis.
How is Bethlem myopathy treated?
The treatment for Bethlem myopathy is symptomatic and supportive. This means that treatment is directed at the symptoms of each affected individual.
There is currently no cure for the disease, and there are no specific medications for Bethlem myopathy. In most cases, physical therapy, stretching exercises, braces, splints, and mobility aids such as a walker or wheelchair may be used to help people with Bethlem myopathy. In rare cases, surgery may be needed to help with joint contractures or scoliosis. Clinical trials are currently testing other possible treatments that could help slow the progression of symptoms of Bethlem myopathy.
Lifestyle changes & home remedies
What are some lifestyle changes or home remedies that can help me manage Bethlem myopathy?
If you have any questions, please consult with your doctor to better understand the best solution for you.
Hello Health Group does not provide medical advice, diagnosis or treatment.
Review Date: February 1, 2018 | Last Modified: February 22, 2018
Bethlem myopathy https://rarediseases.info.nih.gov/diseases/873/bethlem-myopathy Accessed February 01, 2018
What is Bethlem Myopathy, Know it’s Causes, Symptoms, Treatment, Diagnosis https://www.epainassist.com/genetic-disorders/what-is-bethlem-myopathy-know-its-causes-symptoms-treatment-diagnosis Accessed February 01, 2018