ATP1A2 gene mutations are not present in two sisters with basilar-type migraine associated with menses

被引：0

作者：

Cologno, Daniela ^{[1
]}

d'Onofrio, Florindo ^{[2
]}

Esposito, Teresa ^{[3
]}

Gianfrancesco, Fernando ^{[3
]}

Petretta, Vittorio ^{[2
]}

Casucci, Gerardo ^{[4
]}

Frediani, Fabio ^{[5
]}

Buzzi, Maria Gabriella ^{[6
]}

Bussone, Gennaro ^{[7
]}

机构：

[1] Azienda Ospedaliero Univ Osped Riuniti, Inst Clin Neurophysiol, Dept Neurosci, Foggia, Italy

[2] San G Moscati Hosp, Inst Neurol, Avellino, Italy

[3] Italian Natl Res Council, Inst Genet & Biophys, Naples, Italy

[4] Casa Cura S Francesco, Telese, BN, Italy

[5] Inst Neurol, Bergamo, Italy

[6] IRCCS, Santa Lucia Fdn, Rome, Italy

[7] IRCCS C Besta, Inst Neurol, Milan, Italy

来源：

NEUROLOGICAL SCIENCES | 2008年 / 29卷 / 02期

关键词：

basilar-type migraine; ATP1A2; gene; menstrual migraine;

D O I：

10.1007/s10072-008-0870-0

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

Basilar-type migraine (BM) and hemiplegic migraine are clinically distinct subtypes of migraine with aura, however they do share clinical features and it is possible they may share genetic bases. In recent years, ATP1A2 and other gene mutations have been discovered in familial and sporadic hemiplegic migraine. More recently, an ATP1A2 mutation has been identified in an Italian family with BM. In this study we document the absence of ATP1A2 mutations in two Italian sisters with menstrual BM, suggesting that other genes are involved in the condition.

引用

页码：113 / 115

页数：3

共 13 条

[1] ATP1A2 gene mutations are not present in two sisters with basilar-type migraine associated with menses
Daniela Cologno
Florindo d’Onofrio
Teresa Esposito
Fernando Gianfrancesco
Vittorio Petretta
Gerardo Casucci
Fabio Frediani
Maria Gabriella Buzzi
Gennaro Bussone
Neurological Sciences, 2008, 29 : 113 - 115
[2] CACNA1A Nonsense Mutation is Associated With Basilar-Type Migraine and Episodic Ataxia Type 2
Robbins, Matthew S.
Lipton, Richard B.
Laureta, Emma C.
Grosberg, Brian M.
HEADACHE, 2009, 49 (07): : 1042 - 1046
[3] Hemiplegic migraine type 2 with new mutation of the ATP1A2 gene in Japanese cases
Oda, Ituki
Danno, Daisuke
Saigoh, Kazumasa
Wolf, Johanna
Kawashita, Norihito
Hirano, Makito
Samukawa, Makoto
Kitamura, Shigekazu
Kikui, Shoji
Takeshima, Takao
Mitsui, Yoshiyuki
Kusunoki, Susumu
Nagai, Yoshitaka
NEUROSCIENCE RESEARCH, 2022, 180 : 83 - 89
[4] Psychotic aura symptoms in familial hemiplegic migraine type 2 (ATP1A2)
Barros, Jose
Mendes, Alexandre
Matos, Ilda
Pereira-Monteiro, Jose
JOURNAL OF HEADACHE AND PAIN, 2012, 13 (07) : 581 - 585
[5] A novel ATP1A2 gene mutation in familial hemiplegic migraine and epilepsy
Costa, Cinzia
Prontera, Paolo
Sarchielli, Paola
Tonelli, Alessandra
Bassi, Maria Teresa
Cupini, Letizia Maria
Caproni, Stefano
Siliquini, Sabrina
Donti, Emilio
Calabresi, Paolo
CEPHALALGIA, 2014, 34 (01) : 68 - 72
[6] Familial hemiplegic migraine type 2 due to a novel missense mutation in ATP1A2
Fabio Antonaci
Sabrina Ravaglia
Gaetano S. Grieco
Stella Gagliardi
Cristina Cereda
Alfredo Costa
The Journal of Headache and Pain, 2021, 22
[7] A Chinese family with familial hemiplegic migraine type 2 due to a novel missense mutation in ATP1A2
Tang, Wenjing
Zhang, Meichen
Qiu, Enchao
Kong, Shanshan
Li, Yingji
Liu, Huanxian
Dong, Zhao
Yu, Shengyuan
CEPHALALGIA, 2019, 39 (11) : 1382 - 1395
[8] Analysis of chromosome 1 microsatellite markers and the FHM2-ATP1A2 gene mutations in migraine pedigrees
Curtain, RP
Lea, RA
Tajouri, L
Haupt, LM
Ovcaric, M
MacMillan, J
Griffiths, LR
NEUROLOGICAL RESEARCH, 2005, 27 (06) : 647 - 652
[9] Recurrent coma and fever in familial hemiplegic migraine type 2. A prospective 15-year follow-up of a large family with a novel ATP1A2 mutation
Pelzer, N.
Blom, D. E.
Stam, A. H.
Vijfhuizen, L. S.
Hageman, A. T. M.
van Vliet, J. A.
Ferrari, M. D.
van den Maagdenberg, A. M. J. M.
Haan, J.
Terwindt, G. M.
CEPHALALGIA, 2017, 37 (08) : 737 - 755
[10] Two novel mutations of the ATP2C1 gene in Chinese families with Hailey-Hailey disease
Zhu, Ya-Gang
Yang, Sen
Gao, Min
Chen, Jian-Jun
Li, Wei
Wang, Pei-Gang
Zhou, Hai-Lin
Zhao, Xiao-Yan
Ren, Yun-Qing
Xiao, Feng-Li
Du, Wen-Hui
Zhang, Xue-Jun
Zhou, Fu-Sheng
Shen, Yu-Jun
JOURNAL OF DERMATOLOGICAL SCIENCE, 2006, 42 (02) : 125 - 127

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