What is the Difference Between Motor Neuron Disease and Muscular Dystrophy?
🆚 Go to Comparative Table 🆚Motor neuron disease and muscular dystrophy are both neuromuscular diseases, but they differ in the specific areas of the nervous system and muscles they affect.
Motor neuron diseases (MNDs) are a group of progressive neurological disorders that destroy motor neurons, the cells that control skeletal muscle activity such as walking, breathing, speaking, and swallowing. MNDs include diseases such as amyotrophic lateral sclerosis (ALS), progressive bulbar palsy, primary lateral sclerosis, progressive muscular atrophy, spinal muscular atrophy, Kennedy's disease, and post-polio syndrome. MNDs can be inherited or sporadic and typically affect both the central and peripheral nervous systems.
Muscular dystrophy, on the other hand, is a group of inherited diseases characterized by weakness and wasting away of muscle tissue, with or without the breakdown of nerve tissue. There are 9 types of muscular dystrophy, each involving an eventual loss of strength, increasing disability, and possible deformity. The most well-known types are Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD). Muscular dystrophy exclusively affects muscles, not the nervous system.
In summary, the main differences between motor neuron disease and muscular dystrophy are:
- Motor neuron disease affects motor neurons, which control skeletal muscle activity, and can involve both the central and peripheral nervous systems.
- Muscular dystrophy affects muscle tissue and is exclusively hereditary.
Comparative Table: Motor Neuron Disease vs Muscular Dystrophy
Motor Neuron Disease and Muscular Dystrophy are two types of neuromuscular diseases that affect voluntary muscles. Here is a table highlighting the differences between the two:
Feature | Motor Neuron Disease | Muscular Dystrophy |
---|---|---|
Definition | A group of progressive neurological disorders that destroy motor neurons, the cells that control skeletal muscle activity. | A group of inherited diseases characterized by weakness and wasting away of muscle tissue, with or without the breakdown of nerve tissue. |
Cause | Problems in the central nervous system. | Problems in the peripheral nervous system, neuromuscular junction, or skeletal muscle. |
Examples | Amyotrophic Lateral Sclerosis (ALS), Progressive Bulbar Palsy, Primary Lateral Sclerosis, Progressive Muscular Atrophy, Spinal Muscular Atrophy, Kennedy's Disease, and Post-Polio Syndrome. | Duchenne Muscular Dystrophy (DMD), Becker Muscular Dystrophy (BMD), and Oculopharyngeal Muscular Dystrophy. |
Age of Onset | Can affect both children and adults. | Can affect both children and adults. |
Progression | Rare, progressive medical conditions. | Rare, progressive medical conditions. |
Treatment | Specific medicines and supportive therapies. | Specific medicines and supportive therapies. |
While both conditions are neuromuscular diseases and can affect voluntary muscles, motor neuron diseases are caused by problems in the central nervous system, whereas muscular dystrophies are caused by problems in the peripheral nervous system, neuromuscular junction, or skeletal muscle.
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