eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | apraxia |
| Comorbidity | C0039446|telangiectasia |
| Sentences | 2 |
| PubMedID- 20808545 | Other recessive ataxias include ataxia-telangiectasia, ataxia with ocular motor apraxia (aoa), ataxia with vitamin e deficiency (aved), ataxia with coq10 deficiency, abetalipoproteinemia, early-onset cerebellar ataxia with retained tendon reflexes, infantile onset spinocerebellar ataxia, marinesco-sjogren syndrome and spastic ataxia of charlevoix-saguenay [30, 135]. |
| PubMedID- 23538602 | Autosomal recessive ataxias usually have onset in childhood; the most common subtypes are -friedreich, ataxia-telangiectasia, ataxia with oculomotor apraxia type 1, and ataxia with oculomotor apraxia type 2. |
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