Template:Peripheral neuropathy DDX: Difference between revisions
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**[[Amyloidosis]] | **[[Amyloidosis]] | ||
**Chemotherapy-related neuropathy | **Chemotherapy-related neuropathy | ||
**Chronic [[Nitrous oxide toxicity|nitrous oxide abuse]] | |||
**[[Diabetic peripheral neuropathy|Diabetes mellitus]] | **[[Diabetic peripheral neuropathy|Diabetes mellitus]] | ||
**[[Heavy metal toxicity]] | **[[Heavy metal toxicity]] | ||
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**[[Arsenic toxicity]] | **[[Arsenic toxicity]] | ||
**[[Thallium toxicity]] | **[[Thallium toxicity]] | ||
<br>^A condition in which a single nerve is damaged or compressed. | <br>^A condition in which a single nerve is damaged or compressed. | ||
<br>^^A condition where damage to at least two separate peripheral nerves results in a painful, asymmetric, and asynchronous presentation of sensory and motor deficits. | <br>^^A condition where damage to at least two separate peripheral nerves results in a painful, asymmetric, and asynchronous presentation of sensory and motor deficits. | ||
Latest revision as of 06:42, 5 August 2025
Peripheral neuropathy
- Peripheral nerve syndromes (mononeuropathy)^
- Acute trauma
- Chronic nerve entrapment
- Mononeuritis multiplex^^
- Acute
- Diabetes mellitus
- Polyarteritis nodosum
- Connective tissue diseases (e.g., SLE, rheumatoid arthritis)
- Chronic
- Multiple compressive neuropathies
- AIDS
- Sarcoidosis
- Acromegaly
- Leprosy
- Lyme disease
- Idiopathic
- Acute
- Associated with autonomic features
- Alcohol use disorder
- Amyloidosis
- Chemotherapy-related neuropathy
- Chronic nitrous oxide abuse
- Diabetes mellitus
- Heavy metal toxicity
- Porphyria
- Primary dysautonomia
- Vitamin B12 deficiency
- Associated with pain
- Alcohol use disorder
- Amyloidosis
- Chemotherapy (heavy metal toxicity)
- Diabetes mellitus
- Idiopathic polyneuropathy
- Porphyria
- Paraneoplastic syndrome
- Vitamin B1 or B12 deficiency
- Arsenic toxicity
- Thallium toxicity
^A condition in which a single nerve is damaged or compressed.
^^A condition where damage to at least two separate peripheral nerves results in a painful, asymmetric, and asynchronous presentation of sensory and motor deficits.