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2,746 Possible Causes for Polyneuropathy

  • Neuropathy

    Motor Sensory Hereditary Pain Small Fiber Large Fiber Large and Small Fiber Neuronopathy Autonomic Many polyneuropathies have both motor and sensory involvement.[] Robert Rinaldi and Atul Patel, Inherited Polyneuropathies, PM&R, 5, 5S, (S63-S73), (2013).[] Asymmetric Bulbar Cranial Nerve Involvement Proximal Motor Sensory Upper Extremity Many polyneuropathies are: Symmetric Most prominent Distally & in Legs.[]

  • Peripheral Neuropathy

    Motor Sensory Hereditary Pain Small Fiber Large Fiber Large and Small Fiber Neuronopathy Autonomic Many polyneuropathies have both motor and sensory involvement.[] polyneuropathy and (iv) mutilating polyneuropathy with ulcers.[] The variety of HIV-related polyneuropathies will be discussed.[]

  • Polyneuropathy

    (disorder) Polyneuropathy unspecified Polyneuropathy unspecified (disorder) Polyneuropathy, unspecified (disorder) symmetrical polyneuropathy edit English polyneuropathy[] When the cause of polyneuropathy cannot be determined, it is known as idiopathic polyneuropathy. Drug induced polyneuropathy is a result of cancer chemotherapy drugs.[] , of course, the former depends on which polyneuropathy.[]

  • Churg-Strauss Syndrome

    […] clinical and electrophysiological data, 10 (91%) patients demonstrated notable asymmetric involvement, whereas 1 patient presented with a length-dependent symmetrical axonal polyneuropathy[] Further tests verified pulmonary infiltrates, paranasal sinusitis, extravascular eosinophils on histopathologic sample of skin tissue, and polyneuropathy.[] A 58-year-old male presented with sensory motor polyneuropathy and rapidly progressive renal failure.[]

  • Idiopathic Bilateral Vestibulopathy

    Sommer C, Geber C, Young P, Forst R, Birklein F, Schoser B: Polyneuropathies—etiology, diagnosis, and treatment options.[] General features Frequency: 10% to 20% of patients with Sjögren's syndrome May be initial symptom of Sjögren's syndrome No relation to extraneural or serological features Polyneuropathy[] Sommer and colleagues ( 1 ) should be supplemented with information about a recently discovered new facet of toxic polyneuropathy as a side effect of amiodarone ( 2 ).[]

  • Diabetic Polyneuropathy

    Abstract Diabetic polyneuropathy (DPN) has several forms of clinical presentation.[] Electromyoneurography is indispensable in the diagnosis of diabetic polyneuropathy.[] Diabetic polyneuropathy is primarily symmetric sensory neuropathy, initially affecting distal lower extremities.[]

  • Myelitis

    BACKGROUND: HHV7 reactivation has been occasionally reported as a cause of encephalitis or myelitis in transplant recipients, but to our knowledge it has never been associated with neurological disease in HIV-infected patients. We report a case of acute myelitis in an HIV-infected patient, with sustained HHV-7 DNA[…][]

  • Gaucher Disease

    Among them, 10.7% were diagnosed with sensory motor axonal polyneuropathy at baseline using standardized electrophysiological assessment.[] , it was concluded that both prevalence and incidence of polyneuropathy in type 1 GD patients are greater than for the general population.[] Six new cases of polyneuropathy were revealed during two-years monitoring (2.9 per 100 person-years). The same diagnostic procedure was used for the 25 healthy subjects.[]

  • Muscular Atrophy

    The electrodiagnostic examination was compatible with demyelinating sensorimotor polyneuropathy.[] Simultaneous hereditary polyneuropathy and motor neuron disease were suspected and relevant genetic testing was confirmed HNPP and SBMA.[]

  • Hereditary ATTR Amyloidosis

    Familial amyloid polyneuropathy Other names FAP Familial amyloid polyneuropathy has an autosomal dominant pattern of inheritance.[] Specifically, hereditary ATTR amyloidosis with polyneuropathy (hATTR-PN), also referred to as familial amyloidotic polyneuropathy (FAP) is an inherited, progressive, life-threatening[] The two familial forms of this disease are known as familial amyloidotic polyneuropathy (FAP) and familial amyloidotic cardiomyopathy.[]

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