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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease encephalopathy
Comorbidity C0040147|thyroiditis
Sentences 21
PubMedID- 23814544 Although it is usually defined as a corticosteroid-responsive encephalopathy associated with thyroiditis, some patients who suffered from he, responded only to ivig therapy.
PubMedID- 22754574 Steroid response encephalopathy associated with autoimmune thyroiditis (sreat) is a rare disorder first described in 1966. it can present acutely with multiple recurrent focal neurological events or with a progressive, diffuse pattern characterized by cognitive impairment.
PubMedID- 22402791 Seizures are one of the clinical features of encephalopathy associated with autoimmune thyroiditis, often termed hashimoto’s encephalopathy.
PubMedID- 26209970 Steroid responsive encephalopathy associated with autoimmune thyroiditis following ipilimumab therapy: a case report.
PubMedID- 23453127 The misdiagnosis of steroid-responsive encephalopathy associated with autoimmune thyroiditis as masked depression in an elderly euthyroid woman.
PubMedID- 22960439 Autoimmune encephalopathy associated with hashimoto thyroiditis is already known to present with either stroke-like episodes or diffuse progressive deterioration.
PubMedID- 22884222 Elevated anti-thyroperoxidase antibody of 8.07 iu/ml (<5.61 iu/ml) and thyroglobin antibody of 9.85 iu/ml (<4.11 iu/ml) were found and steroid responsive encephalopathy associated with autoimmune thyroiditis was diagnosed.
PubMedID- 23748728 Steroid-responsive encephalopathy associated with autoimmune thyroiditis (sreat), also known as hashimoto encephalopathy, represents a rare disorder of presumed autoimmune origins that can be diagnosed when a protean variety of psychiatric symptoms are present in association with elevated titers of anti-thyroid antibodies.
PubMedID- 24598831 Aim: steroid responsive encephalopathy with autoimmune thyroiditis (sreat) is a clinically and electrographically heterogeneous steroid-responsive encephalopathy associated with thyroid autoantibodies.
PubMedID- 25982498 Steroid-responsive autoimmune encephalopathy associated with autoimmune thyroiditis (sreat) presenting with myoclonus-dystonia syndrome.
PubMedID- 23605832 Extensively elevated thyroid-antibodies in the serum and csf, as well as the rapid and sustained recovery after intravenous treatment with prednisolone, pointed to the diagnosis of a primarily psychiatric manifestation of a steroid responsive encephalopathy associated with autoimmune thyroiditis (sreat).
PubMedID- 25084973 Steroid-responsive encephalopathy associated with autoimmune thyroiditis (sreat): case report of reversible coma and status epilepticus in an adolescent patient and review of the literature.
PubMedID- 21763957 Seizures of unknown etiology are a common presenting sign in the pediatric intensive care unit, and steroid-responsive encephalopathy with autoimmune thyroiditis should be considered as a possible cause of recurrent seizures.
PubMedID- 20831030 Steroid responsive encephalopathy associated with autoimmune thyroiditis presenting with late onset depression.
PubMedID- 25963777 In the majority of cases, other more or less subtle findings, such as magnetic resonance imaging (mri), electroencephalography (eeg) pathology, or neurological soft signs point to an “organic cause” of the psychotic syndrome; however, a number of case reports in the literature indicate that ie is identified in psychotic cases without these findings [3] (endres d, perlov e, stich o, tebartz van elst l: steroid responsive encephalopathy associated with autoimmune thyroiditis (sreat) - presenting as major depression, in preparation).
PubMedID- 21397101 Background: steroid responsive encephalopathy associated with autoimmune thyroiditis (sreat) is a condition of presumed autoimmune etiology that can present with a variety of neuropsychiatric signs and symptoms.
PubMedID- 25667846 This disorder, which is also called steroid-responsive encephalopathy associated with autoimmune thyroiditis (sreat), was first described by brain et al.
PubMedID- 22827897 Some investigators proposed the term “steroid-responsive encephalopathy associated with autoimmune thyroiditis (sreat)” [1] to replace “hashimoto’s encephalopathy”.
PubMedID- 22030535 Recurrent partial seizures with ictal yawning as atypical presentation of hashimoto's encephalopathy (steroid-responsive encephalopathy associated with autoimmune thyroiditis).
PubMedID- 25487777 In addition to whipple's disease, myorhythmia has been described in patients with cerebrovascular disease, listeria encephalitis, anti-n-methyl-d-aspartate receptor encephalitis, steroid-responsive encephalopathy associated with autoimmune thyroiditis, multiple sclerosis, and other disorders.
PubMedID- 24633901 Steroid responsive encephalopathy with autoimmune thyroiditis (sreat), a rare disorder in individuals of all age groups, including children, is characterized by high titers of anti-thyroid peroxidase antibodies.

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