Disease A-Z Library

Rx Neurology (A – Z)

Browse plain-English disease and condition guides, including symptoms, causes, diagnosis, treatment options, prevention, and when to seek medical care.

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Diseases A-Z

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Disease A-Z Library

Paraneoplastic Motor Neuropathy

Paraneoplastic Motor Neuropathy is a rare, immune-driven attack on the motor nerves that control voluntary muscle movement. It happens because the body tries to fight a...

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Disease A-Z Library

Toxic Motor Neuropathy

Toxic motor neuropathy is a nerve-damage disorder in which chemicals, drugs, or biological toxins selectively attack the motor fibers that control muscle movement. Unlike diabetic or...

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Diabetic Motor Neuropathy

Diabetic motor neuropathy is a form of nerve damage that strikes the big motor nerves powering your muscles rather than (or long before) the small sensory...

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Distal Hereditary Motor Neuropathy

Distal Hereditary Motor Neuropathy—often shortened to dHMN—is a group of inherited nerve disorders in which the longest, most distant motor nerves slowly degenerate. Motor nerves carry...

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Distal Axonal Motor Neuropathy

Distal Axonal Motor Neuropathy (often shortened to DAMN or simply “distal motor axonal neuropathy”) is a nerve-wasting disorder in which the long, thin extensions (axons) of...

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Critical-Illness Motor Axonopathy (CIMA)

Critical-Illness Motor Axonopathy (CIMA) is the pure motor, axonal form of the broader syndrome called critical-illness polyneuropathy and myopathy (CIP/CIM). In CIMA, the long “wires” (axons)...

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Paraneoplastic Motor Neuropathy

Paraneoplastic Motor Neuropathy (PMN) is a rare, immune-mediated nerve disorder triggered by an underlying, often hidden cancer. It causes slowly progressive limb weakness, muscle wasting, and...

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Multifocal Motor Neuropathy (MMN)

MMN, sometimes called “multifocal motor neuropathy with conduction block,” is an autoimmune peripheral neuropathy. In plain English, your body’s defence system mistakenly produces antibodies (most often...

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Occipital Horn Syndrome (OHS)

Occipital Horn Syndrome (OHS) is a rare, inherited connective-tissue and copper-transport disorder caused by harmful changes (pathogenic variants) in the ATP7A gene on the X-chromosome. Because...

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