In nutritional neuropathies, the peripheral nerves, which branch from the brain and spinal cord, are damaged by deficiencies of essential nutrients, particularly those of the vitamin B complex.

Worldwide, nutritional neuropathies are generally caused by malnutrition. In developed countries, such neuropathies are more commonly associated with excessive alcohol consumption. People who drink heavily often also have a poor diet, which can cause a vitamin B deficiency. In addition, alcohol may directly damage the peripheral nerves. A person who has been drinking heavily for 10 years or more has a greatly increased risk of developing a nutritional neuropathy.

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Nutritional deficiencies may occur in people with eating disorders, such as anorexia nervosa. People with long-term conditions that affect absorption of nutrients from the intestines may also develop nutritional deficiencies.

What are the symptoms?

Nutritional neuropathies usually first affect the tips of the fingers and the toes. The symptoms appear gradually over several months or years and slowly progress up the limbs to the trunk. Symptoms may include:

- Loss of sensation.
- Pins and needles.
- Pain in the feet and/or the hands.

Walking may be clumsy as a result of the loss of sensation in the feet and legs.

If the motor nerves (nerves that stimulate the muscles) are affected, muscle weakness and wasting may develop and further affect the ability to walk.

What might be done?

Your doctor will examine you by checking your reflexes and your ability to feel sensation such as a pin prick. He or she may arrange for blood tests to look for a vitamin deficiency or for evidence of liver damage caused by excessive alcohol consumption. Your doctor may also arrange for tests that measure the extent of the nerve damage.

Nutritional neuropathies are treated by replacing the missing nutrients. This is done either by giving a course of oral supplements or, in some cases, by injections. Your doctor may also prescribe anticonvulsant drugs or antidepressants to help to control the symptoms. You may also be prescribed painkillers to relieve any discomfort. Nerve damage is usually irreversible, but with treatment the progression of the disease can usually be halted.

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In diabetic neuropathy, one or more of the peripheral nerves that branch from the brain and spinal cord to the rest of the body are damaged as a result of diabetes mellitus. Diabetic neuropathy is the most common cause of peripheral neuropathy in developed countries. If diabetes is poorly controlled, it results in high levels of glucose in the blood that damage the peripheral nerves directly and the blood vessels that supply them. Good control of diabetes reduces this risk by up to half.

About 3 in 10 people with diabetes mellitus have damage to one or more peripheral nerves, but only 1 of these 3 people develops significant symptoms.

People with diabetes mellitus who smoke increase the risk of damaging the blood vessels that supply the nerves,

What are the symptoms?

The symptoms of diabetic neuropathy usually develop slowly over a number of years. Rarely, they develop rapidly over days or weeks. Symptoms vary depending on which nerves are involved, but the feet are frequently affected. Less commonly, diabetic neuropathy may affect the larger nerves, mainly in the thighs. Symptoms may include:

- Pins and needles.
- Numbness.
- Pain, which is often worse at night.
- Muscle weakness and wasting.

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In sensation is lost, a minor injury to the foot, such as rubbing by badly fitting shoes, may not be noticed. Slow healing due to poor blood supply may lead to infection. If left untreated, ulcers may develop and, in severe cases, gangrene occurs.

Eventually, diabetic neuropathy may also affect the autonomic nerves that regulate automatic body functions such as blood pressure control and digestion. Damage to these nerves causes symptoms such as dizziness when standing, diarrhea, and impotence.

What might be done?

Careful control of diabetes reduces the risk of developing diabetic neuropathy. However, if you develop symptoms of nerve damage, you should consult your doctor. He or she will probably be able to diagnose the condition from your symptoms. However, nerve conduction tests may need to be carried out in hospital to confirm which nerves are affected and to assess the severity of the damage. The goal of treatment of diabetic neuropathy is to prevent further nerve damage and the development of complications. Your doctor will help you to monitor your blood sugar level carefully and advise you about good foot care. For example, you should check your feet regular for cuts or abrasions, particularly if you have been wearing new shoes. You should avoid wearing open-toed sandals or walking barefoot. If you smoke, you should try to give up.

To relive pain, particularly at night, certain anticonvulsant drugs, such as carbamazepine and phenytoin, or an antidepressant drug, such as amitriptyline, may be prescribed.

What is the prognosis?

Good control of blood glucose levels in diabetes mellitus not only reduces the risk of developing diabetic neuropathy but may also half further progression of the disease. However, in most cases, nerve damage is irreversible.

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Disorders of the peripheral nerves, the nerves that branch from the brain and spinal cord to the rest of the body, are called neuropathies. Depending on the nerves affected, peripheral neuropathies may affect sensation, movement, or automatic functions, such as bladder control. Rarely, a peripheral neuropathy may be life-threatening.

What are the causes?

In developed countries, the most common cause of damage to the peripheral nerves is diabetes mellitus. Vitamin B complex deficiencies and some nutritional disorders may also result in nerve damage. In the developed world, nutritional neuropathy is often the result of a poor diet in people who abuse alcohol. Drinking too much alcohol may also damage peripheral nerves directly.

Damage to a single nerve may occur as a result of an injury or because of compression. For example, in carpal tunnel syndrome, the median nerve, which supplies that part of the hand, is compressed at the wrist.

Neuropathy may also be associated with an infection, such as Hansen’s disease or HIV infection. Guilain-Barre syndrome, a neuropathy that is rapidly progressive, is caused by an abnormal immune response that sometimes occurs after an infection.

Autoimmune disorders such as systemic lupus erythematosus, in which the immune system attacks the body’s tissues, may cause nerve damage occasionally, a disorder such as polyarteritis nodosamay damage nerves by causing inflammation of the blood vessels that supply them. Neuropathy may also result from certain cancers, particularly primary lung cancer and lymphoma. Occasionally, neuropathy is caused by amyloidosis, in which an abnormal protein is deposited in the body.

Some drugs, such as isoniazid, may cause nerve damage, as may exposure to certain toxic substances, such as lead. In some cases, the cause is unknown.

A painless ulcer developing under the big toe joint due to peripheral neuropathy

What are the types?

Peripheral neuropathies may affect the nerves that transmit sensory information (sensory nerves), the nerves that stimulate the muscles (motornerves), and/or the nerves that control automatic functions (autonomic nerves).

Sensory nerve neuropathies: these neuropathies first affect the hands and feet and the spread towards the centre of the body. The symptoms may include tingling, pain, and numbness in the affected area. If the fingertips are numb, everyday tasks may become difficult. This type of neuropathy is most often caused by nutritional disorders or drugs.

Motor nerve neuropathies: if the motor nerves are damaged, the muscles they supply become weak, and wasting occurs eventually. In severe cases, mobility may become restricted, and very rarely, breathing may have to be assisted by mechanical ventilation. Lead poisoning may result in a neuropathy that affects the motor nerves only.

Autonomic nerve neuropathies: a neuropathy that is affecting one or more autonomic nerves may result in constipation, fainting due to low blood pressure, diarrhoea, urinary in continence, or impotence. This type of neuropathy is often caused by long-standing diabetes mellitus.

What might be done?

Your doctor may be able to tell which nerves are affected from your symptoms and an examination. If the cause of your neuropathy is not clear, he or she will probably arrange for blood tests to look for evidence of an underlying disorder, such as nutritional deficiencies or an autoimmune disorder. If Mere is evidence of compression of a nerve, you may also have CT scanning or MRI to assess the severity and extent of nerve damage. Special tests to assess the function of the nerves may also be carried out.

The treatment of a peripheral neuropathy depends on the cause and the type of nerve affected. For example, careful control of diabetes mellitus may keep diabetic neuropathy from worsening, and vitamin B complex injections may help a nutritional neuropathy. If motor nerves are affected, you may have physiotherapy to help to maintain muscle tone. Wearing a foot splint may assist walking. Sometimes, the underlying cause can be treated, but long-standing nerve damage may be irreversible.


TEST NERVE AND MUSLCE ELECTRICAL TESTS

Nerve and muscle electrical test consist of nerve conduction studies and electromyography (EMG). Nerve conduction studies are used to assess how well a nerve is conducting electrical impulses. They are often followed by EMG to see whether symptoms, such as weakness, are due to a disorder of the muscle or the nerve supplying it. Both tests are usually done on an outpatient basis. Each takes about 15 minutes and may cause discomfort.

Nerve conduction studies

Nerve conduction studies are carried out to assess nerve damage in disorders such as peripheral neuropathies. A nerve is stimulated by an electrical impulse, and the response to the stimulus and the speed at which this response travels along the nerve indicates whether the nerve is damaged and the nature and extent of the damage.

Electromyography

EMG is used to differentiate between nerve and muscle disorders and to diagnose disorders such as muscular dystrophy. A fine needle is used to record the electrical activity of a muscle at rest and when contracting. The results are recorded on a trace.

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Multiple sclerosis (MS) is the most common nervous system disorder affecting young adults. In this condition, nerves in the brain and spinal cord are progressively damaged, causing a wide range of symptoms that affect sensation, movement, body functions, and balance. Specific symptoms may relate to the particular areas that are damaged and vary in severity between individuals. For example, damage to the optic nerve may cause blurred vision. If nerve fibres in the spinal cord are affected, it may cause weakness and heaviness in the legs or arms. Damage to nerves in the brain stem, the area of the brain that connects to the spinal cord, may affect balance.

In many people with MS, symptoms occur intermittently and there may be long periods of remission. However, some people have chronic (long-term) symptoms that gradually get worse.

In the UK, about 85,000 people are affected by MS. People who have a close relative with MS are more likely to develop the disorder. The condition is much more common in the northern hemisphere, which suggests that environmental factors also play a part. MS is more common in females and the disorder is more likely develop between early adulthood and middle age.

What are the causes?

MS is an autoimmune disorder, in which the body’s immune system attacks its own tissue, in this case those of the nervous system. Many nerves in the brain and spinal cord are covered by a protective insulating sheath of material called myelin. In MS, small areas of myelin are damaged, leaving holes in the sheath, a process known as demyelination. Once the myelin sheath has been damaged, impulses cannot be conducted normally along nerves to and from the brain and spinal cord. At first, the damage may be limited to only one nerve, but myelin covering other nerves may become damaged over time. Eventually, damaged parches of myelin insulation are replaced by scar tissue.

It is thought that MS may be triggered by external factors such as a viral infection during childhood in genetically susceptible individuals.

What are the types?

There are two types of MS. In the most common, known as relapsing remitting MS, symptoms last for days or weeks and then clear up for months or even years. However, some symptoms may eventually persist between the attacks. About 3 in 10 people with MS have a type known as chronic-progressive MS, in which there is a gradual worsening of symptoms with no remission.

A person with relapsing-remitting MS may go on to develop chronic-progressive MS.

What are the symptoms?

Symptoms may occur singly in the initial stages and in combination as the disorder progresses. They may include:

- Blurred vision.
- Numbness or tingling in any part of the body.
- Tiredness, which may be persistent.
- Weakness and a feeling of heaviness in the legs or arms.
- Problems with coordination and balance, such as an unsteady gait.

Stress and heat sometimes make symptoms worse. About half of the people who have MS find it hard to concentrate and experience memory lapses. Depression is common. Later in the course of the disease, some people with muscle weakness develop painful muscle spasms. Spinal cord damage can lead to urinary incontinence, and men may have increasing difficulty in achieving an erection. Eventually, damage to myelin covering nerves in the spinal cord may cause partial paralysis, and an affected person may need a wheelchair.

How is it diagnosed?

There is no single test to diagnose MS, and, because symptoms are so wide-ranging, a diagnosis is only made once other possible causes of the symptoms have been excluded. Your doctor will take your medical history and carry out a physical examination. If you are having visual problems, such as blurred vision, you may be referred to an ophthalmologist, who will assess the optic nerve, which is commonly affected in the early stages of the disorder. Your doctor may arrange for tests to find out how quickly your brain receives messages when particular nerves are stimulated. The most common test measures damage to the visual pathways. You will probably also have an imaging test of the brain, such as MRI, to see if there are areas of demyelination.

Your doctor may arrange for a lumbar puncture, a procedure in which a small amount of the fluid that surrounds the spinal cord is removed for microscopic analysis. Abnormalities in this fluid may confirm the diagnosis.

What is the treatment?

There is no cure for MS, but if you have relapsing-remitting MS, interferon beta may help to lengthen remission periods and shorten the length of attacks. Your doctor may also prescribe corticosteroids to shorten the duration of a relapse. However, at present, there is no specific treatment to halt the progression of chronic-progressive MS.

Many of the more common symptoms that occur in all types of MS can be relieved by drugs. For example, your doctor may treat muscle spasms with a drug that relaxes muscles. Similarly, incontinence can often be improved by drugs. Problems in getting an erection may be helped by a drugs treatment such as sildenafil. If you have mobility problems, your doctor may arrange for you to have physiotherapy. Occupational therapy may make day-to-day activities easier.

What can I do?

If you are diagnosed with MS, you and your family will need time and possibly counseling to come to terms with the disorder. You should minimize stress in your life and avoid exposure to high temperatures if hear tends to make your symptoms worse. Regular, gentle exercise, such as swimming, will help to keep your muscle strong without the risk of overstraining them.

The progression of MS is extremely variable, but people who are older when the disease first develops tend to fare less well. About 7 in 10 people with MS have active lives with long periods of remission between relapses. However, some people, particularly those with chronic-progressive MS, become increasingly disabled. Half of all people with MS are still leading active lives 10 years after diagnosis, and the average lifespan from diagnosis is 25-30 years.


VISUAL EVOKED RESPONSES

A visual evoked response test measure the function of the optic nerve, the nerve that transmits messages from the eye to the brain. The test is most often used to in the diagnosis of multiple sclerosis and can detect abnormalities even if visual symptoms are not apparent. The test records brain activity in response to a visual stimulus to find out the speed at which messages from the eye reach the brain. The test takes 20-30 minutes.

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Motor neuron disease is rare, affecting 1-2 people in every 100,000 worldwide each year. In this disease, also known as amyotrophic lateral sclerosis, degeneration of the nerves involved in muscular activity results in progressive wasting of the muscles and weakness. There are several types of motor neuron disease. Some affect mainly the spinal nerves, while other types also affect the brain. The condition is not painful, does not affect bowel or bladder function, and does not usually affect the intellect or the senses, such as sight.

Steven Hawkins is the one of few people to ever live passed 5 years with MND. 

He has lived for around 40 years

The cause of motor neuron disease is unknown. Genetic factors are involved because, in about 1 in 10 cases, the disease runs in the family. The disease is slightly more common in men and usually develops after the age of 40.

What are the symptoms?

Initially, weakness and wasting develop over a few months and usually affect the muscles of the hands, arms, or legs. Other early symptoms may include:

- Twitching movements in the muscles.
- Stiffness and muscle cramps.
- Difficulty in carrying out twisting movements, such as unscrewing bottle tops and turning keys.

As the disease progresses, other symptoms may include:

- Dragging one foot or a tendency to stumble when walking.
- Difficulty in climbing stairs or getting up from low chairs.

Less commonly, the muscles of the mouth and throat are involved, and may cause slurred speech, hoarseness, and difficulty in swallowing.

An affected person may have mood swings and may become anxious and depressed. If the muscles involved in breathing and swallowing are affected, small particles of food may enter the lungs and cause recurrent chest infections and possibly pneumonia. The head may fall forwards because the muscles in the neck are too weak to support it. Eventually, weakness of the muscles that control respiration may cause difficulty in breathing.

How is diagnosed?

There is no specific test to diagnose motor neuron disease. However, electromyography may be carried out to detect a decrease in electrical activity in the muscles. Additional tests may be used to exclude other possible causes of the symptoms. For example, MRI or CT scanning of the brain and neck may be used to exclude a local problem such as a tumour or cervical spondylosis.

What is the treatment?

At present, no treatment can significantly slow down the progression of motor neuron disease, although a new drug called riluzole may have a small effect. Treatment for symptoms may include antidepressants to relieve depression and antibiotics to treat chest infections. If the person is having difficulty in swallowing, a gastrostomy maybe created surgically. This is an opening through which a permanent feeding tube is inserted directly into the stomach or the small intestine.

Usually, a team of specialists provide support and care for an affected person and members of the family. Counseling may be offered to both. The person affected by the disease may have physiotherapy to keep joints and muscles supple and may be given aids to help with activities such as eating and walking. A speech therapist can supply communication aids to help with speech difficulties and advise on swallowing problems. Joining a self-help group is often helpful to person with motor neuron disease and his or her family.

The outlook for motor neuron disease is variable, with approximately 2 in 10 affected people alive 5 years after diagnosis. About 1 in 10 affected people survives more than 10 years.

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