eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | carnitine deficiency, systemic primary |
| Symptom | C0085584|encephalopathy |
| Sentences | 5 |
| PubMedID- 22294053 | We hypothesize that observed improvement related to the resolution of reversible metabolic encephalopathy and myopathy associated with secondary carnitine deficiency. |
| PubMedID- 22258360 | Acquired encephalopathy associated with carnitine deficiency after cefditoren pivoxil administration. |
| PubMedID- 22846666 | carnitine deficiency presenting with encephalopathy and hyperammonemia in a patient receiving chronic enteral tube feeding: a case report. |
| PubMedID- 24612242 | Mri findings in encephalopathy with primary carnitine deficiency: a case report. |
| PubMedID- 26336183 | She was diagnosed with valproate-induced encephalopathy due to carnitine deficiency. |
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