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PedAM

Pediatric Disease Annotations & Medicines




Disease encephalopathy
Phenotype C0040147|thyroiditis
Sentences 24
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- 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- 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- 22030535 Recurrent partial seizures with ictal yawning as atypical presentation of hashimoto's encephalopathy (steroid-responsive encephalopathy associated with autoimmune thyroiditis).
PubMedID- 26209970 Conclusion: steroid responsive encephalopathy associated with autoimmune thyroiditis may be a hitherto unrecognized complication of ipililumab treatment and should be taken into consideration in patients developing central nervous symptoms undergoing this treatment.
PubMedID- 20831030 Steroid responsive encephalopathy associated with autoimmune thyroiditis presenting with late onset depression.
PubMedID- 22754574 Steroid response encephalopathy associated with autoimmune thyroiditis (sreat), or hashimoto's encephalopathy, is a rare disorder believed to be immune-mediated.
PubMedID- 24454425 He is known as steroid-responsive encephalopathy associated with autoimmune thyroiditis (1–3).
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- 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- 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- 22402791 Seizures are one of the clinical features of encephalopathy associated with autoimmune thyroiditis, often termed hashimoto’s encephalopathy.
PubMedID- 23453127 The misdiagnosis of steroid-responsive encephalopathy associated with autoimmune thyroiditis as masked depression in an elderly euthyroid woman.
PubMedID- 22827897 Some investigators proposed the term “steroid-responsive encephalopathy associated with autoimmune thyroiditis (sreat)” [1] to replace “hashimoto’s encephalopathy”.
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- 25084973 Steroid-responsive encephalopathy associated with autoimmune thyroiditis (sreat), also termed hashimoto's encephalopathy (he), is a rare immune-mediated disorder and is also affecting children and adolescents.
PubMedID- PMC4480949 Steroid-responsive encephalopathy associated with autoimmune thyroiditis (sreaat) represents another form of encephalopathic disorder associated with thyroid disease and causing potentially serious clinical complications.
PubMedID- 22960439 Autoimmune encephalopathy associated with hashimoto thyroiditis is already known to present with either stroke-like episodes or diffuse progressive deterioration.
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.
PubMedID- 25667846 This disorder, which is also called steroid-responsive encephalopathy associated with autoimmune thyroiditis (sreat), was first described by brain et al.
PubMedID- 26441585 Moreover, steroid responsive encephalopathy associated with autoimmune thyroiditis (sreat) has received an increased level of interest in recent years because it was identified as the cause for classical psychotic and affective disorders in several cases (castillo et al., 2006).
PubMedID- 25982498 Steroid-responsive autoimmune encephalopathy associated with autoimmune thyroiditis (sreat) presenting with myoclonus-dystonia syndrome.
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- 24598831 Steroid responsive encephalopathy associated with autoimmune thyroiditis (sreat) in childhood.

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