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94 Possible Causes for Mild Sensorimotor Peripheral Neuropathy

  • Peripheral Neuropathy

    Our clinical assessment did not highlight obvious clinical features supporting a peripheral neuropathy but evidence of mild proximal weakness.[ncbi.nlm.nih.gov] Electrophysiological studies performed at our hospital revealed evidence of a sensorimotor demyelinating polyneuropathy with possible axonal involvement.[ncbi.nlm.nih.gov]

  • X-linked Parkinsonism-Spasticity Syndrome

    NCV showed a mixed, but primarily axonal sensorimotor peripheral neuropathy with low sensory amplitudes and normal conduction speed, and low motor amplitudes and delayed conduction[journals.plos.org] MRI of the brain revealed cerebellar atrophy and mild atrophy of the corpus callosum ( Figure 2 ), whereas MRI of the spine and cord was normal.[journals.plos.org]

  • Paraneoplastic Syndrome

    Peripheral neuropathy is the most common neurologic paraneoplastic syndrome.[merckmanuals.com] Mild distal sensorimotor neuropathies are quite common in patients with cancer and are not necessarily paraneoplastic—other factors to consider include metabolic, nutritional[doi.org] Subacute sensory neuropathy is a more specific but rare peripheral neuropathy.[merckmanuals.com]

  • Cold-Induced Sweating Syndrome Type 2

    Crisponi/cold-induced sweating syndrome is an autosomal recessive disorder characterized in the neonatal period by orofacial weakness with impaired sucking and swallowing resulting in poor feeding necessitating medical intervention. Affected infants show a tendency to startle, with contractions of the facial muscles[…][diseaseinfosearch.org]

  • Spastic Paraplegia

    NCV showed a mixed, but primarily axonal sensorimotor peripheral neuropathy with low sensory amplitudes and normal conduction speed, and low motor amplitudes and delayed conduction[journals.plos.org] MRI of the brain revealed cerebellar atrophy and mild atrophy of the corpus callosum ( Figure 2 ), whereas MRI of the spine and cord was normal.[journals.plos.org]

  • Familial Amyloid Polyneuropathy

    These signs include a history of carpal tunnel syndrome, sensorimotor peripheral neuropathy, unexplained intense myalgias and burning sensations, and autonomic dysfunction[ojrd.biomedcentral.com] Careful evaluation for these signs is mandatory, as they can sometimes be very mild and may not be reported by the patient.[ojrd.biomedcentral.com]

  • Cranial Neuropathy

    Neurological recovery was slow; the patient continues to have a mild peripheral sensorimotor neuropathy three years after the onset of the illness.[ncbi.nlm.nih.gov] A 15-year-old boy is described with Epstein-Barr virus infection complicated by prolonged life-threatening thrombocytopenia, cranial neuropathy and peripheral sensorimotor[ncbi.nlm.nih.gov] neuropathy.[ncbi.nlm.nih.gov]

  • Hereditary Sensory Neuropathy

    It is the most commonly inherited peripheral neuropathy in the UK. Lifespan is normal. Disability is usually mild.[gpnotebook.co.uk] neuropathy.[gpnotebook.co.uk] […] site is intended for healthcare professionals General Practice Notebook Charcot-Marie-Tooth disease is an autosomal dominant condition characterised by slowly progressive sensorimotor[gpnotebook.co.uk]

  • Hereditary Motor and Sensory Neuropathy

    […] denervation, NCV decreased CMT: CHARCOT MARIE TOOTH (HMSN-1) Gen: AD, Ch17, PMP22 (peripheral myelin protein) accumulates Epi: adolescent Sx: distal sensorimotor neuropathy[learnneurosurgery.com] […] collagen layers @ axons ( onion bulb) Sx: nerves enlarge, palpable (hypertrophic neuropathy) Distal weak / numb (claw hand, feet high arch, hammer toes, decreased DTRs) EMG: mild[learnneurosurgery.com]

  • Charcot-Marie-Tooth Disease Type 2S

    […] a peripheral sensorimotor neuropathy, characterized by distal legs sensory loss and weakness that can be asymmetric.[ebi.ac.uk] OLS Orphanet Rare Disease Ontolog ORDO Orphanet:228174 Autosomal dominant Charcot-Marie-Tooth disease type 2N (CMT2N) is a mild form of axonal Charcot-Marie-Tooth disease,[ebi.ac.uk]

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