(G60.0) Hereditary motor and sensory neuropathy

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127 032 in individuals diagnosis hereditary motor and sensory neuropathy confirmed

4 684 deaths with diagnosis hereditary motor and sensory neuropathy

4% mortality rate associated with the disease hereditary motor and sensory neuropathy

Etiology Pathogenesis Clinical Pattern Diagnostics Treatment Prevention

Diagnosis hereditary motor and sensory neuropathy is diagnosed Men are 3.18% more likely than Women

65 533

Men receive the diagnosis hereditary motor and sensory neuropathy

2 433 (3.7 %)

Died from this diagnosis.

100

61 499

Women receive the diagnosis hereditary motor and sensory neuropathy

2 251 (3.7 %)

Died from this diagnosis.

Risk Group for the Disease hereditary motor and sensory neuropathy - Men and Women aged 10-14

In Men diagnosis is most often set at age 0-94

Less common in men the disease occurs at Age 95+Less common in women the disease occurs at Age 0-1, 90-94

In Women diagnosis is most often set at age 0-89, 95+

Disease Features hereditary motor and sensory neuropathy

Absence or low individual and public risk

Hereditary motor and sensory neuropathy - what does this mean

Hereditary motor and sensory neuropathy is a genetic disorder that affects the peripheral nervous system, causing damage to the nerves in the arms and legs. it is caused by mutations in various genes that affect the production of proteins that are important for the maintenance and functioning of the peripheral nerves. symptoms of the disorder include muscle weakness and atrophy, loss of sensation, and pain in the hands and feet.

What happens during the disease - hereditary motor and sensory neuropathy

Hereditary motor and sensory neuropathy is a genetic disorder caused by a mutation in one of several genes that are responsible for the production of proteins that form the myelin sheath that insulates and protects the nerve cells in the body. this mutation causes a decrease in myelin production, leading to damage to the nerve cells and the inability of the nerves to effectively transmit signals to the muscles and other body tissues. this results in the motor and sensory symptoms associated with this disorder, such as weakness, numbness, and tingling.

Clinical Pattern

More details coming soon

How does a doctor diagnose

Complete physical examination
Neurological examination
Blood tests
Nerve conduction studies
Electromyography (EMG)
Genetic testing
Imaging studies such as MRI and CT scans
Muscle biopsy

Treatment and Medical Assistance

Main goal: Improve the quality of life of the patient

Pain management
Physical therapy
Occupational therapy
Balance training
Stretching exercises
Restorative therapies
Medication to reduce nerve pain
Assistive devices (e.g. walkers, canes, braces)
Nutritional supplements
Surgery (e.g. nerve transfers, tendon transfers)

18 Days of Hospitalization Required

Average Time for Outpatient Care Not Established

Hereditary motor and sensory neuropathy - Prevention

Hereditary motor and sensory neuropathy can be prevented by avoiding environmental risk factors that may trigger the disease, such as smoking, alcohol, and drug use. additionally, regular physical activity, a healthy diet, and adequate rest can help to reduce the risk of developing the condition.

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