Literature DB >> 16628531

Sporadic and familial hemiplegic migraine: diagnosis and treatment.

David F Black1.   

Abstract

Hemiplegic migraine is a rare subtype of migraine with aura associated with transient hemiplegia. The weakness is caused by motor aura. Hemiplegic migraine is the only headache syndrome associated with known genetic mutations and serves as a model for understanding more common varieties of migraine. Because the phenotype includes striking yet transient neurological signs and symptoms, it is imperative that clinicians know the differential diagnosis to rule out possible secondary etiologies when treating patients with hemiplegic spells. Hemiplegic migraine occurs with equal prevalence in either a sporadic or familial form differentiated only by family history. Thus far, treatment trials are anecdotal, although verapamil and acetazolamide have shown promise.

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Year:  2006        PMID: 16628531     DOI: 10.1055/s-2006-939921

Source DB:  PubMed          Journal:  Semin Neurol        ISSN: 0271-8235            Impact factor:   3.420


  9 in total

1.  Hemiplegic migraine with reversible cerebral vasoconstriction caused by ATP1A2 mutations.

Authors:  Andreas Hermann; Kay Engelandt; Bernd Rautenstrauss; Heinz Reichmann; Eleonore Jacobasch
Journal:  J Neurol       Date:  2013-07-03       Impact factor: 4.849

Review 2.  Mutational consequences of aberrant ion channels in neurological disorders.

Authors:  Dhiraj Kumar; Rashmi K Ambasta; Pravir Kumar
Journal:  J Membr Biol       Date:  2014-08-14       Impact factor: 1.843

3.  Sporadic Hemiplegic Migraine with ATP1A2 and Prothrombin Gene Mutations.

Authors:  Jose Aceves; Diana Mungall; Batool F Kirmani
Journal:  Case Rep Neurol Med       Date:  2013-12-11

4.  Use of acetazolamide in sulfonamide-allergic patients with neurologic channelopathies.

Authors:  Daniel Platt; Robert C Griggs
Journal:  Arch Neurol       Date:  2011-12-12

5.  Familial hemiplegic migraine in a child with seizure disorder: clinical history is the key to diagnosis.

Authors:  Pranav Balakrishnan; Phalguna Kousika Katakam; Asha P Hegde
Journal:  BMJ Case Rep       Date:  2019-03-25

6.  Case Report: Recurrent Hemiplegic Migraine Attacks Accompanied by Intractable Hypomagnesemia Due to a de novo TRPM7 Gene Variant.

Authors:  Meifang Lei; Ping Wang; Hong Li; Xiaojun Liu; Jianbo Shu; Qianqian Zhang; Chunquan Cai; Dong Li; Yuqin Zhang
Journal:  Front Pediatr       Date:  2022-05-31       Impact factor: 3.569

7.  A mutation in the first intracellular loop of CACNA1A prevents P/Q channel modulation by SNARE proteins and lowers exocytosis.

Authors:  Selma A Serra; Ester Cuenca-León; Artur Llobet; Francisca Rubio-Moscardo; Cristina Plata; Oriel Carreño; Noèlia Fernàndez-Castillo; Roser Corominas; Miguel A Valverde; Alfons Macaya; Bru Cormand; José M Fernández-Fernández
Journal:  Proc Natl Acad Sci U S A       Date:  2010-01-08       Impact factor: 11.205

8.  An acute stroke CT imaging algorithm incorporating automated perfusion analysis.

Authors:  Danielle Byrne; John P Walsh; Peter J MacMahon
Journal:  Emerg Radiol       Date:  2019-02-01

9.  Migraine associated cerebral hyperperfusion with arterial spin-labeled MR imaging.

Authors:  J M Pollock; A R Deibler; J H Burdette; R A Kraft; H Tan; A B Evans; J A Maldjian
Journal:  AJNR Am J Neuroradiol       Date:  2008-05-22       Impact factor: 3.825

  9 in total

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