Coincidence of familial hemiplegic migraine and hemicrania continua? A case report

被引：18

作者：

Evers, S ^{[1
]}

Bahra, A

Goadsby, PJ

机构：

[1] Univ London, Dept Clin Neurol, Inst Neurol, London, England

[2] UCL Natl Hosp Neurol & Neurosurg, London WC1N 3BG, England

来源：

CEPHALALGIA | 1999年 / 19卷 / 05期

基金：

英国惠康基金;

关键词：

D O I：

10.1046/j.1468-2982.1999.019005533.x

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

A case is presented of a 39-year-old woman with a history of simultaneous Familial hemiplegic migraine (FHM) and hemicrania continue (HC). The family history of the patient revealed different types of migraine and cyclic syndromes in childhood in four generations. The possible links between FHM and HC are discussed. The pedigree gives further evidence that cyclic syndromes in childhood belong to the spectrum of migraine.

引用

页码：533 / 535

页数：3

共 16 条

[1] CHRONIC PAROXYSMAL HEMICRANIA (CPH) - A REVIEW OF THE CLINICAL MANIFESTATIONS [J].

ANTONACI, F ;

SJAASTAD, O .

HEADACHE, 1989, 29 (10) :648-656

[2]

Antonaci F, 1992, Funct Neurol, V7, P471

[3] HEMICRANIA CONTINUA - A CLINICAL REVIEW [J].

BORDINI, C ;

ANTONACI, F ;

STOVNER, LJ ;

SCHRADER, H ;

SJAASTAD, O .

HEADACHE, 1991, 31 (01) :20-26

[4] Coexistence of migraine and cluster headache: Report of 10 cases and possible pathogenetic implications [J].

DAmico, D ;

Centonze, V ;

Grazzi, L ;

Leone, M ;

Ricchetti, G ;

Bussone, G .

HEADACHE, 1997, 37 (01) :21-25

[5] A review of paroxysmal hemicranias, SUNCT syndrome and other short-lasting headaches with autonomic feature, including new cases [J].

Goadsby, PJ ;

Lipton, RB .

BRAIN, 1997, 120 :193-209

[6] Episodic ataxia and channelopathies [J].

Gordon, N .

BRAIN & DEVELOPMENT, 1998, 20 (01) :9-13

[7] FAMILIAL HEMIPLEGIC MIGRAINE IN THE NETHERLANDS [J].

HAAN, J ;

TERWINDT, GM ;

BOS, PLJM ;

OPHOFF, RA ;

FRANTS, RR ;

FERRARI, MD ;

LINDHOUT, DL ;

SANDKUYL, LA ;

VANEYK, R .

CLINICAL NEUROLOGY AND NEUROSURGERY, 1994, 96 (03) :244-249

[8]

JOUTEL A, 1994, AM J HUM GENET, V55, P1166

[9] GENETIC-HETEROGENEITY OF FAMILIAL HEMIPLEGIC MIGRAINE [J].

OPHOFF, RA ;

VANEIJK, R ;

SANDKUIJL, LA ;

TERWINDT, GM ;

GRUBBEN, CPM ;

HAAN, J ;

LINDHOUT, D ;

FERRARI, MD ;

FRANTS, RR .

GENOMICS, 1994, 22 (01) :21-26

[10] Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4 [J].

Ophoff, RA ;

Terwindt, GM ;

Vergouwe, MN ;

vanEijk, R ;

Oefner, PJ ;

Hoffman, SMG ;

Lamerdin, JE ;

Mohrenweiser, HW ;

Bulman, DE ;

Ferrari, M ;

Haan, J ;

Lindhout, D ;

vanOmmen, GJB ;

Hofker, MH ;

Ferrari, MD ;

Frants, RR .

CELL, 1996, 87 (03) :543-552

← 1 2 →