PedAM
Pediatric Disease Annotations & Medicines
| Disease | neuropathy |
| Phenotype | C0029089|ophthalmoplegia |
| Sentences | 9 |
| PubMedID- 23147504 | Most patients have sensory-motor neuropathy, sometimes associated with ophthalmoplegia, ataxia, seizures, parkinsonism, myopathy, or visceral disorders. |
| PubMedID- 22616202 | Sensory ataxic neuropathy with dysarthria/dysphagia and ophthalmoplegia (sando). |
| PubMedID- 26176228 | A case of a 2-year-old boy undergoing treatment for leukemia who developed sudden onset bilateral ptosis and ophthalmoplegia along with generalized neuropathy due to vincristine's neurotoxic effects is presented. |
| PubMedID- 26331046 | The predominant features of mfs are ophthalmoplegia and ataxia, with a peripheral neuropathy being only a very mild clinical feature. |
| PubMedID- 23649749 | Chronic ataxic neuropathy with ophthalmoplegia, igm paraprotein, cold agglutinins, and anti-disialyl antibodies (canomad) was diagnosed. |
| PubMedID- 21896416 | The clinical and laboratory features have been described under the acronym canomad: chronic ataxic neuropathy with ophthalmoplegia, m proteins, cold agglutinins and disialosyl antibodies. |
| PubMedID- 22006700 | The acronym canomad encompasses chronic ataxic neuropathy combined with ophthalmoplegia, m protein, cold agglutinins, and anti-disialosyl antibodies.herein we describe 2 patients presenting with progressive ataxic neuropathy who only developed ophthalmoplegia after a significant delay post-presentation, which in 1 case had features indicative of brainstem dysfunction. |
| PubMedID- 21087783 | Common physiological pathways are involved in several arca, such as dna repair deficiency (aoa1, ataxia telangiectasia [at]...), rna termination disorder (aoa2), mitochondrial defect (frda, sensory ataxic neuropathy with dysarthria and ophthalmoplegia [sando]...), lipoprotein assembly defects (aved, abetalipoproteinemia [abl]), chaperon protein disorders (arsacs, marinesco-sjogren syndrome [mss]) or peroxysomal diseases (refsum disease [rd]). |
| PubMedID- 24291973 | Fisher syndrome has been regarded peculiar inflammatory neuropathy with ophthalmoplegia, ataxia, and areflexia, whereas bickerstaff brainstem encephalitis has been considered pure central nervous system disease characterized with ophthalmoplegia, ataxia, and consciousness disturbance. |
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