Kennedy's disease
Kennedy’s disease
Kennedy’s disease is a rare inherited neuromuscular disorder that causes progressive weakening and wasting of the muscles, particularly the arms and legs. Other major symptoms include severe cramps and problems with speech and swallowing. The disease progresses slowly, and life expectancy is usually normal. Kennedy’s disease is also known as X-linked spinal bulbar muscular atrophy (SBMA). There is no cure yet, and treatment can only ease some of the symptoms.
In most cases, females who inherit the gene are carriers, while men who inherit the gene develop the symptoms. (Rarely, an affected woman may develop symptoms too.)
Symptoms of Kennedy’s disease
The many symptoms of Kennedy’s disease generally first appear when the person is aged between 30 and 50 years and can include:
swallowing difficulties
speech difficulties
hand tremors
shaky muscles when holding certain postures
muscle weakness
muscle wastage
muscle twitches
muscle cramps and spasms
enlarged calf muscles due to constant cramping
localised areas of numbness
absent reflexes, such as the foot remaining still when the tendon beneath the kneecap is tapped
enlarged breast tissue (gynaecomastia)
impotence
low sperm count
shrunken testicles
reduced sex drive.
Kennedy’s disease destroys motor nerves
The brain controls the movement of muscles with nerves. The command to move travels from the upper motor neurons on the brain’s surface, down through the spinal cord and into the lower motor neurons. Every muscle is connected to between 50 and 200 lower motor neurones, and each neurone subdivides into many tiny branches. The end of each branch is called a pre-synaptic terminal. The electrical command to move the muscle is translated at the pre-synaptic terminal into a chemical called acetylcholine, which prompts special receptors in the muscle tissue to contract.
Kennedy’s disease causes the loss of motor neurone cells, including those in the brain stem that supply the bulbar muscles. These muscles control the throat, which is why swallowing, breathing and speech problems are common symptoms of Kennedy’s disease.
This inherited disorder affects males
Humans have 46 paired chromosomes, with two sex chromosomes that decide gender and 44 chromosomes that dictate other factors. The mother’s egg always provides a female sex chromosome known as ‘X’, while the father’s sperm contributes either an ‘X’ (female) or ‘Y’ (male) chromosome. A pairing of ‘XX’ sex chromosomes means the baby is a girl, while ‘XY’ means the baby is a boy. Kennedy’s disease is caused by a genetic mutation of the androgen receptor gene on the X chromosome.
Since the disease is recessive, the presence of the normal gene on the other X chromosome means that girls don’t develop the symptoms of disease, because the normal gene overrides the mutated one. However, these girls will be carriers, and each son of a carrier mother has a 50 per cent chance of inheriting the gene and developing the disease. This is because boys only receive one X chromosome and, if that has the mutated gene, they will one day develop the symptoms of Kennedy’s disease.
The androgen receptor gene
The androgen receptor gene helps to control the activity of the male sex hormones (androgens). This explains the androgen insensitivity symptoms such as breast enlargement, impotence and low sperm count. However, it is not known why this gene mutation causes the other symptoms of Kennedy’s disease.
Diagnosis of Kennedy’s disease
Since Kennedy’s disease is rare, it can be misdiagnosed. It is sometimes mistaken for the more common motor neurone disease (amyotrophic lateral sclerosis), a progressive nervous system disease characterised by the breaking down of neurones in the spinal cord and brain.
Kennedy’s disease can be diagnosed using a number of tests including:
Blood test to check for elevated serum creatine kinase (CPK)
– people with Kennedy’s disease usually have a greater than average amount of this particular enzyme circulating in their blood.
Genetic tests using a blood sample
– this test can check whether the Kennedy’s disease gene is present, even if the person is asymptomatic or a carrier. Genetic counselling is important.
Treatment for Kennedy’s disease
There is no cure for Kennedy’s disease, because medical science doesn’t know how to regenerate muscle neurones. Treatment aims to ease some of the symptoms and can include:
medications to reduce muscle cramps and tremors
plenty of rest and avoidance of exhaustion
healthy, balanced diet
gentle and regular aerobic exercise
regular stretching to help reduce muscle cramping
pain management
speech therapy
occupational therapy
physiotherapy.
Where to get help
Your
GP (doctor)
MND
Victoria
External Link
Tel:
1800 777 175
Victorian Clinical Genetic
Services
External Link
Tel.
1300 118 247