Literature DB >> 4041774

Migraine coma. Meningitic migraine with cerebral oedema associated with a new form of autosomal dominant cerebellar ataxia.

R B Fitzsimons, W H Wolfenden.   

Abstract

A family with hemiplegic migraine has been documented for a period of over forty years. From this study and the literature we conclude that (1) migraine is a cause of recurrent coma which may be associated with life-threatening cerebral hemisphere oedema; (2) hyperpyrexia with CSF pleocytosis occurs in hemiplegic migraine, which may thus simulate viral meningoencephalitis; and (3) cerebral angiography is hazardous in hemiplegic migraine and may exacerbate coma and cerebral oedema. In the family reported, cerebellar ataxia was present during recovery from attacks of hemiplegic migraine and affected patients ultimately suffered from persistent ataxia with radiological cerebellar atrophy. This syndrome thus constitutes a distinct form of late-onset autosomal dominant cerebellar ataxia and also of familial periodic ataxia. The status of 'cerebellar migraine' is reviewed.

Entities:  

Mesh:

Year:  1985        PMID: 4041774     DOI: 10.1093/brain/108.3.555-a

Source DB:  PubMed          Journal:  Brain        ISSN: 0006-8950            Impact factor:   13.501


  20 in total

1.  Migraine coma.

Authors:  D Corbin; T Martyr; A C Graham
Journal:  J Neurol Neurosurg Psychiatry       Date:  1991-08       Impact factor: 10.154

Review 2.  Single gene disorders causing ischaemic stroke.

Authors:  Saif S M Razvi; Ian Bone
Journal:  J Neurol       Date:  2006-06       Impact factor: 4.849

3.  Familial migraine coma: a case study.

Authors:  T F Münte; H Müller-Vahl
Journal:  J Neurol       Date:  1990-02       Impact factor: 4.849

4.  Head injury induced migraine coma simulating acute extradural intracranial haemorrhage.

Authors:  R Duncan; A Jenkins
Journal:  J Neurol Neurosurg Psychiatry       Date:  1989-06       Impact factor: 10.154

Review 5.  The cerebellum and migraine.

Authors:  Maurice Vincent; Nouchine Hadjikhani
Journal:  Headache       Date:  2007-06       Impact factor: 5.887

Review 6.  Toward a molecular genetic classification of familial hemiplegic migraine.

Authors:  Joost Haan; Esther E Kors; Arn M J M van den Maagdenberg; Kaate R J Vanmolkot; Gisela M Terwindt; Rune R Frants; Michel D Ferrari
Journal:  Curr Pain Headache Rep       Date:  2004-06

Review 7.  Pseudomigraine with lymphocytic pleocytosis.

Authors:  Julio Pascual; Natalia Valle
Journal:  Curr Pain Headache Rep       Date:  2003-06

8.  The S218L familial hemiplegic migraine mutation promotes deinhibition of Ca(v)2.1 calcium channels during direct G-protein regulation.

Authors:  Norbert Weiss; Alejandro Sandoval; Ricardo Felix; Arn Van den Maagdenberg; Michel De Waard
Journal:  Pflugers Arch       Date:  2008-06-26       Impact factor: 3.657

9.  A G301R Na+/K+ -ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs.

Authors:  Maria Spadaro; Simona Ursu; Frank Lehmann-Horn; Liana Veneziano; Veneziano Liana; Giovanni Antonini; Antonini Giovanni; Paola Giunti; Giunti Paola; Marina Frontali; Karin Jurkat-Rott
Journal:  Neurogenetics       Date:  2004-07-31       Impact factor: 2.660

10.  [Trauma-triggered migraine attacks. Review of the literature.].

Authors:  W Trabert; U Thoden
Journal:  Schmerz       Date:  1991-06       Impact factor: 1.107

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.