Neuropathy
Motor Sensory Hereditary Pain Small Fiber Large Fiber Large and Small Fiber Neuronopathy Autonomic Many polyneuropathies have both motor and sensory involvement.[neuromuscular.wustl.edu]
Robert Rinaldi and Atul Patel, Inherited Polyneuropathies, PM&R, 5, 5S, (S63-S73), (2013).[dx.doi.org]
Asymmetric Bulbar Cranial Nerve Involvement Proximal Motor Sensory Upper Extremity Many polyneuropathies are: Symmetric Most prominent Distally & in Legs.[neuromuscular.wustl.edu]
Peripheral Neuropathy
Motor Sensory Hereditary Pain Small Fiber Large Fiber Large and Small Fiber Neuronopathy Autonomic Many polyneuropathies have both motor and sensory involvement.[neuromuscular.wustl.edu]
polyneuropathy and (iv) mutilating polyneuropathy with ulcers.[ncbi.nlm.nih.gov]
The variety of HIV-related polyneuropathies will be discussed.[ncbi.nlm.nih.gov]
Polyneuropathy
(disorder) Polyneuropathy unspecified Polyneuropathy unspecified (disorder) Polyneuropathy, unspecified (disorder) symmetrical polyneuropathy edit English polyneuropathy[wikidata.org]
When the cause of polyneuropathy cannot be determined, it is known as idiopathic polyneuropathy. Drug induced polyneuropathy is a result of cancer chemotherapy drugs.[symptoma.com]
, of course, the former depends on which polyneuropathy.[en.wikipedia.org]
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[ncbi.nlm.nih.gov]
Further tests verified pulmonary infiltrates, paranasal sinusitis, extravascular eosinophils on histopathologic sample of skin tissue, and polyneuropathy.[ncbi.nlm.nih.gov]
A 58-year-old male presented with sensory motor polyneuropathy and rapidly progressive renal failure.[ncbi.nlm.nih.gov]
Idiopathic Bilateral Vestibulopathy
Sommer C, Geber C, Young P, Forst R, Birklein F, Schoser B: Polyneuropathies—etiology, diagnosis, and treatment options.[aerzteblatt.de]
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[neuromuscular.wustl.edu]
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 ).[aerzteblatt.de]
Diabetic Polyneuropathy
Abstract Diabetic polyneuropathy (DPN) has several forms of clinical presentation.[ncbi.nlm.nih.gov]
Electromyoneurography is indispensable in the diagnosis of diabetic polyneuropathy.[ncbi.nlm.nih.gov]
Diabetic polyneuropathy is primarily symmetric sensory neuropathy, initially affecting distal lower extremities.[ncbi.nlm.nih.gov]
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[…][ncbi.nlm.nih.gov]
Gaucher Disease
Among them, 10.7% were diagnosed with sensory motor axonal polyneuropathy at baseline using standardized electrophysiological assessment.[content.sciendo.com]
, it was concluded that both prevalence and incidence of polyneuropathy in type 1 GD patients are greater than for the general population.[content.sciendo.com]
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.[content.sciendo.com]
Muscular Atrophy
The electrodiagnostic examination was compatible with demyelinating sensorimotor polyneuropathy.[ncbi.nlm.nih.gov]
Simultaneous hereditary polyneuropathy and motor neuron disease were suspected and relevant genetic testing was confirmed HNPP and SBMA.[ncbi.nlm.nih.gov]
Hereditary ATTR Amyloidosis
Familial amyloid polyneuropathy Other names FAP Familial amyloid polyneuropathy has an autosomal dominant pattern of inheritance.[en.wikipedia.org]
Specifically, hereditary ATTR amyloidosis with polyneuropathy (hATTR-PN), also referred to as familial amyloidotic polyneuropathy (FAP) is an inherited, progressive, life-threatening[alnylam.microartswpdev.com]
The two familial forms of this disease are known as familial amyloidotic polyneuropathy (FAP) and familial amyloidotic cardiomyopathy.[symptoma.com]