Neurologic and other systemic manifestations in FMF: Published and own experience
Familial Mediterranean fever (FMF) is an autosomal recessive autoinflammatory disease, presenting with recurrent episodes of fever and polyserositis. Neurologic involvement in FMF is rare and usually considered fortuitous. The aim of this article is to review the spectrum of possible neurologic mani...
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Published in | Best practice & research. Clinical rheumatology Vol. 26; no. 1; pp. 119 - 133 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier Ltd
01.02.2012
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Subjects | |
Online Access | Get full text |
ISSN | 1521-6942 1532-1770 1532-1770 |
DOI | 10.1016/j.berh.2012.01.004 |
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Abstract | Familial Mediterranean fever (FMF) is an autosomal recessive autoinflammatory disease, presenting with recurrent episodes of fever and polyserositis. Neurologic involvement in FMF is rare and usually considered fortuitous. The aim of this article is to review the spectrum of possible neurologic manifestations, which can be encountered in FMF patients, and to establish their relation to FMF.
We reviewed the literature based on Pubmed search to find neurologic manifestations, which were reported in FMF patients. To that we added our own experience on the subject, abstracted from our computerised FMF registry of 12000 FMF patients of the National FMF Center and the computerised database of Sheba Medical Center.
A wide range of neurologic manifestations involving FMF patients was noted. A large part of these manifestations could be directly related to FMF, its complications, associated diseases and treatment adverse effects. The remaining were incidental, or of uncertain association to FMF.
A physician, taking care of an FMF patient, can face various neurologic manifestations and should be aware of their origin. The current chapter provides an insight to this association of FMF. |
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AbstractList | Objective Familial Mediterranean fever (FMF) is an autosomal recessive autoinflammatory disease, presenting with recurrent episodes of fever and polyserositis. Neurologic involvement in FMF is rare and usually considered fortuitous. The aim of this article is to review the spectrum of possible neurologic manifestations, which can be encountered in FMF patients, and to establish their relation to FMF. Methods We reviewed the literature based on Pubmed search to find neurologic manifestations, which were reported in FMF patients. To that we added our own experience on the subject, abstracted from our computerised FMF registry of 12000 FMF patients of the National FMF Center and the computerised database of Sheba Medical Center. Results A wide range of neurologic manifestations involving FMF patients was noted. A large part of these manifestations could be directly related to FMF, its complications, associated diseases and treatment adverse effects. The remaining were incidental, or of uncertain association to FMF. Conclusion A physician, taking care of an FMF patient, can face various neurologic manifestations and should be aware of their origin. The current chapter provides an insight to this association of FMF. Familial Mediterranean fever (FMF) is an autosomal recessive autoinflammatory disease, presenting with recurrent episodes of fever and polyserositis. Neurologic involvement in FMF is rare and usually considered fortuitous. The aim of this article is to review the spectrum of possible neurologic manifestations, which can be encountered in FMF patients, and to establish their relation to FMF. We reviewed the literature based on Pubmed search to find neurologic manifestations, which were reported in FMF patients. To that we added our own experience on the subject, abstracted from our computerised FMF registry of 12000 FMF patients of the National FMF Center and the computerised database of Sheba Medical Center. A wide range of neurologic manifestations involving FMF patients was noted. A large part of these manifestations could be directly related to FMF, its complications, associated diseases and treatment adverse effects. The remaining were incidental, or of uncertain association to FMF. A physician, taking care of an FMF patient, can face various neurologic manifestations and should be aware of their origin. The current chapter provides an insight to this association of FMF. Familial Mediterranean fever (FMF) is an autosomal recessive autoinflammatory disease, presenting with recurrent episodes of fever and polyserositis. Neurologic involvement in FMF is rare and usually considered fortuitous. The aim of this article is to review the spectrum of possible neurologic manifestations, which can be encountered in FMF patients, and to establish their relation to FMF.OBJECTIVEFamilial Mediterranean fever (FMF) is an autosomal recessive autoinflammatory disease, presenting with recurrent episodes of fever and polyserositis. Neurologic involvement in FMF is rare and usually considered fortuitous. The aim of this article is to review the spectrum of possible neurologic manifestations, which can be encountered in FMF patients, and to establish their relation to FMF.We reviewed the literature based on Pubmed search to find neurologic manifestations, which were reported in FMF patients. To that we added our own experience on the subject, abstracted from our computerised FMF registry of 12000 FMF patients of the National FMF Center and the computerised database of Sheba Medical Center.METHODSWe reviewed the literature based on Pubmed search to find neurologic manifestations, which were reported in FMF patients. To that we added our own experience on the subject, abstracted from our computerised FMF registry of 12000 FMF patients of the National FMF Center and the computerised database of Sheba Medical Center.A wide range of neurologic manifestations involving FMF patients was noted. A large part of these manifestations could be directly related to FMF, its complications, associated diseases and treatment adverse effects. The remaining were incidental, or of uncertain association to FMF.RESULTSA wide range of neurologic manifestations involving FMF patients was noted. A large part of these manifestations could be directly related to FMF, its complications, associated diseases and treatment adverse effects. The remaining were incidental, or of uncertain association to FMF.A physician, taking care of an FMF patient, can face various neurologic manifestations and should be aware of their origin. The current chapter provides an insight to this association of FMF.CONCLUSIONA physician, taking care of an FMF patient, can face various neurologic manifestations and should be aware of their origin. The current chapter provides an insight to this association of FMF. |
Author | Yahalom, G. Feld, O. Livneh, A. |
Author_xml | – sequence: 1 givenname: O. surname: Feld fullname: Feld, O. email: Feld.family@gmail.com organization: FMF Clinic and Department of Medicine F, Sheba Medical Center, Ramat Gan, Tel-Hashomer 52621, Israel – sequence: 2 givenname: G. surname: Yahalom fullname: Yahalom, G. email: Gyahalom@gmail.com organization: Department of Neurology, Sheba Medical Center, Ramat Gan, Tel-Hashomer 52621, Israel – sequence: 3 givenname: A. surname: Livneh fullname: Livneh, A. email: alivneh@post.tau.co.il, alivneh@sheba.health.gov.il organization: FMF Clinic and Department of Medicine F, Sheba Medical Center, Ramat Gan, Tel-Hashomer 52621, Israel |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/22424198$$D View this record in MEDLINE/PubMed |
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Keywords | Central nervous system vasculitis Aseptic meningitis Neurologic manifestations Stroke Demyelinating diseases PRES (posterior reversible leukoencephalopathy) FMF (familial Mediterranean fever) Colchicine Seizures Cognitive impairment |
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Snippet | Familial Mediterranean fever (FMF) is an autosomal recessive autoinflammatory disease, presenting with recurrent episodes of fever and polyserositis.... Objective Familial Mediterranean fever (FMF) is an autosomal recessive autoinflammatory disease, presenting with recurrent episodes of fever and polyserositis.... |
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SubjectTerms | Aseptic meningitis Brain Diseases - diagnosis Central nervous system vasculitis Cognition Disorders - diagnosis Cognitive impairment Colchicine Demyelinating diseases Demyelinating Diseases - diagnosis Familial Mediterranean Fever - diagnosis FMF (familial Mediterranean fever) Humans Meningitis, Aseptic - diagnosis Neurologic manifestations Posterior Leukoencephalopathy Syndrome - diagnosis PRES (posterior reversible leukoencephalopathy) Rheumatology Seizures Seizures - diagnosis Stroke Stroke - diagnosis Vasculitis, Central Nervous System - diagnosis |
Title | Neurologic and other systemic manifestations in FMF: Published and own experience |
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