ENCEFALITE LIMBICA PDF

Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. For all other comments, please send your remarks via contact us. Only comments written in English can be processed. This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications. Detailed information.

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Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. For all other comments, please send your remarks via contact us. Only comments written in English can be processed. A rare limbic encephalitis characterized by the presence of autoantibodies against NMDA receptors in serum and cerebrospinal fluid.

It may be of paraneoplastic most commonly associated with ovarian teratoma or non-paraneoplastic origin and is life-threatening but potentially treatable. Patients present with acute behavioral change, psychosis, and catatonia, rapidly progressing to seizures, memory deficit, dyskinesias, speech problems, and autonomic and breathing dysregulation.

Other search option s Alphabetical list. Suggest an update. Summary and related texts. Related genes. Clinical signs. Check this box if you wish to receive a copy of your message. Disease definition A rare limbic encephalitis characterized by the presence of autoantibodies against NMDA receptors in serum and cerebrospinal fluid.

Detailed information Article for general public Svenska Professionals Review article English Clinical practice guidelines Deutsch Additional information Further information on this disease Classification s 1 Gene s 0 Other website s 0. Health care resources for this disease Expert centres Diagnostic tests 8 Patient organisations 47 Orphan designation s and orphan drug s 0. Specialised Social Services Eurordis directory.

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.

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Autoimmune limbic encephalitis ALE associated with systemic lupus erythematosus SLE is a rare entity with few reports in the literature to date. In general, ALE associated with SLE has a satisfactory response to immunosuppressive treatment RIT , but the pathogenesis of this association is poorly understood and may include an autoimmunity component. We report a case study describing the diagnosis and management of limbic encephalitis in a patient with active Systemic Lupus Erythematosus disease SLE and past medical history of cancer endometrial adenocarcinoma in and papillary urothelial carcinoma in with curative treatment , followed over a one-year period. We discuss the possible association between limbic encephalitis and all past neoplastic and immune-mediated conditions of this patient.

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Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. For all other comments, please send your remarks via contact us. Only comments written in English can be processed. A rare limbic encephalitis characterized by the presence of autoantibodies against NMDA receptors in serum and cerebrospinal fluid. It may be of paraneoplastic most commonly associated with ovarian teratoma or non-paraneoplastic origin and is life-threatening but potentially treatable.

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