dc.contributor.author |
Gungor, S |
|
dc.contributor.author |
Raif, SG |
|
dc.date.accessioned |
2022-10-13T11:45:41Z |
|
dc.date.available |
2022-10-13T11:45:41Z |
|
dc.date.issued |
2015 |
|
dc.identifier.uri |
http://hdl.handle.net/11616/79060 |
|
dc.description.abstract |
Hashimoto encephalopathy is a rare syndrome in children with nonspecific clinical symptoms, which leads to underdiagnosis. Encephalopathy with a high thyroperoxidase antibody levels and exclusion of other causes can provide a diagnosis unrelated to thyroid hormone status. An acute, subacute, chronic, progressive, or relapsing-remitting course can be seen. The main therapy for Hashimoto encephalopathy is steroid administration, which lends its other name as steroid-responsive encephalopathy associated with autoimmune thyroiditis. However, there are few cases with spontaneous remission without steroid therapy. Here, we report a case with a relapsing course but spontaneous remission. |
|
dc.description.abstract |
C1 [Gungor, Serdal; Raif, Sabiha G.] Inonu Univ, Fac Med, Dept Pediat Neurol, Malatya, Turkey. |
|
dc.source |
JOURNAL OF PEDIATRIC EPILEPSY |
|
dc.title |
Relapsing-Remitting Encephalopathy with Status Epilepticus: Think |
|
dc.title |
Hashimoto Encephalopathy |
|