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43 Possible Causes for Mild Axonal Peripheral Neuropathy

  • Mitochondrial Trifunctional Protein Deficiency

    RESULTS: Despite normal sensory examination, nerve conduction studies showed a mild axonal peripheral neuropathy.[ncbi.nlm.nih.gov] Childhood- or adolescent-onset recurrent rhabdomyolysis is a common muscular manifestation and is preceded frequently by clinically overt peripheral neuropathy.[ncbi.nlm.nih.gov]

  • Lyme Disease

    Abstract The tick-borne spirochetes that cause Lyme disease in North America and Eurasia display strong linkage disequilibrium between certain chromosomal and plasmid loci within each three major geographic areas of their distribution. For strain typing for epidemiologic and ecologic purposes, the commonly used[…][ncbi.nlm.nih.gov]

  • Oculomotor Apraxia

    Brain magnetic resonance imaging showed cerebellar atrophy and mild brainstem atrophy. Electromyography showed signs of axonal neuropathy.[ncbi.nlm.nih.gov] We describe two siblings, born to consanguineous parents, who had clinical features of cerebellar ataxia, tremor, dysarthria, oculomotor apraxia, and motor peripheral neuropathy[ncbi.nlm.nih.gov]

  • Spinocerebellar Ataxia with Rigidity and Peripheral Neuropathy

    […] sensorimotor peripheral neuropathy with axonal and demyelinating elements in six of ten German patients with SCA6. 1 Thus, peripheral neuropathy appears to be more frequent[ams.ac.ir] […] a severe primary motor peripheral axonal motor neuropathy.[medcraveonline.com] Nerve conduction studies showed mild axonal motor sensory neuropathy in his lower limbs; the patient refused to undergo detailed electromyographic examination.[pmj.bmj.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]

  • Inherited Neuropathy

    Charcot-Marie-Tooth hereditary neuropathy type 2 (CMT2) is a non-demyelinating (axonal) peripheral neuropathy characterized by distal muscle weakness and atrophy, mild sensory[bcbst.com] ., peripheral myelin protein 22) gene.[bcbst.com]

  • Miller-Fisher Syndrome

    Nerve conduction studies were indicative of a predominantly axonal sensori-motor peripheral neuropathy.[ncbi.nlm.nih.gov] Neurological examination revealed a bilateral external ophthalmoplegia, dysphagia, dysarthria, mild shoulder girdle muscle weakness and gait ataxia, accompanied by absent[ncbi.nlm.nih.gov]

  • Bezafibrate

    The neurophysiological evidence suggested a mild peripheral sensory neuropathy of an axonal type, the apparent discrepancy between the results of nerve conduction studies[bmj.com]

  • Distal Hereditary Motor Neuropathy Type 5

    Charcot-Marie-Tooth hereditary neuropathy type 2 (CMT2) is a non-demyelinating (axonal) peripheral neuropathy characterized by distal muscle weakness and atrophy, mild sensory[bcbst.com] ., peripheral myelin protein 22) gene.[bcbst.com]

  • Distal Hereditary Motor Neuropathy Type 2C

    Charcot-Marie-Tooth hereditary neuropathy type 2 (CMT2) is a non-demyelinating (axonal) peripheral neuropathy characterized by distal muscle weakness and atrophy, mild sensory[bcbst.com] ., peripheral myelin protein 22) gene.[bcbst.com]

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