| HMSN | Hereditary Motor-Sensory Neuropathy |
|---|---|
| AION | anterior ischemic optic neuropathy |
| AN | acanthosis nigricans; acne neonatorum; acoustic neuroma; adult, normal; ala nasi; amyl nitrate; aneu... |
| BPN | bacitracin, polymyxin B, neomycin sulfate; brachial plexus neuropathy |
| CSNA | congenital sensory neuropathy with anhidrosis [syndrome] |
| peripheral neuropathy | <neurology> Injury to the nerves that supply sensation to the arms and legs. Origin: Gr. Pathos = disease (16 Dec 1997) |
|---|---|
| chronic interstitial hypertrophic neuropathy | dejerine-Sottas disease |
| motor dapsone neuropathy | A peripheral neuropathy due to ingestion of 4,4-deaminodiphenylsulphone. (05 Mar 2000) |
| compression neuropathy | A focal nerve lesion produced when sustained pressure is applied to a localised portion of the nerve, either from an external or internal source; the main source of injury is the pressure differential that exists between one portion of the nerve and another. (05 Mar 2000) |
| heavy metal neuropathy | Peripheral nervous system disorders attributed to intoxication of one of the heavy metals: arsenic, gold, lead, mercury, platinum and thallium. (05 Mar 2000) |
| hereditary hypertrophic neuropathy | dejerine-Sottas disease |
| hereditary sensory radicular neuropathy | Neuropathy characterised by the occurrence of severe, relapsing foot ulcerations of neuropathic origin, destruction of terminal digits of feet and hands, and a loss of sensation; autosomal dominant inheritance is associated with onset in the second decade or later. (05 Mar 2000) |
| hypertrophic interstitial neuropathy | Sensorimotor neuropathy characterised pathologically by collections of Schwann cell processes arranged concentrically around one or more nerve fibres. No genetic factors are known in its aetiology.For hereditary types, see hereditary hypertrophic neuropathy. (05 Mar 2000) |
| neuropathy | <clinical sign> A general term denoting functional disturbances and/or pathological changes in the peripheral nervous system. If the involvement is in one nerve it is called mononeuropathy, in several nerves, mononeuropathy multiplex, if diffuse and bilateral, polyneuropathy. The aetiology may be known for example arsenical neuropathy, diabetic neuropathy, ischaemic neuropathy, traumatic neuropathy) or unknown. Encephalopathy and myelopathy are corresponding terms relating to involvement of the brain and spinal cord, respectively. The term is also used to designate noninflammatory lesions in the peripheral nervous system, in contrast to inflammatory lesions (neuritis). Origin: Gr. Pathos = disease (18 Nov 1997) |
| dapsone neuropathy | A peripheral neuropathy that develops in patients taking dapsone (4,4-diaminodiphenylsulfone); unusual features include being a pure motor neuropathy, and beginning in the hands, sometimes asymmetrically. (05 Mar 2000) |
| symmetric distal neuropathy | <neurology> A disease process involving a number of peripheral nerves. Origin: Gr. Pathos = disease (14 Oct 1997) |
| diabetic neuropathy | <neurology, pathology> Long standing or poorly controlled diabetes can cause permanent peripheral and autonomic nerve dysfunction known as diabetic neuropathy. Origin: Gr. Pathos = disease (27 Sep 1997) |
| diphtheritic neuropathy | A rapidly developing peripheral neuropathy caused by a toxin elaborated by Corynebacterium diphtheriae. (05 Mar 2000) |
| ischemic neuropathy | Neuropathy resulting from acute or chronic ischemia of the involved nerves. (05 Mar 2000) |
| ischemic optic neuropathy | Optic nerve neuropathy secondary to hypoperfusion of the low pressure posterior ciliary arteries supplying the optic nerve head (nonarteritic) or to temporal arteritis (arteritic). (05 Mar 2000) |