A Missense Mutation in the MBTPS2 Gene Underlies the X-Linked Form of Olmsted Syndrome

被引:43
作者
Haghighi, Alireza [1 ]
Scott, Claire A. [2 ]
Poon, Daniel S. [2 ]
Yaghoobi, Reza [3 ]
Saleh-Gohari, Nasrollah [4 ]
Plagnol, Vincent [5 ]
Kelsell, David P. [2 ]
机构
[1] Univ Oxford, Nuffield Dept Clin Med, Wellcome Trust Ctr Human Genet, Oxford, England
[2] Queen Mary Univ London, Barts & London Sch Med & Dent, Ctr Cutaneous Res, Blizard Inst, London, England
[3] Ahvaz Jundishapur Univ Med Sci, Dept Dermatol, Ahvaz, Iran
[4] Kerman Univ Med Sci, Dept Genet, Kerman, Iran
[5] UCL, Genet Inst, London, England
关键词
IFAP SYNDROME; CLEAVAGE; FOLLICULARIS; PROTEIN;
D O I
10.1038/jid.2012.289
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
引用
收藏
页码:571 / 573
页数:3
相关论文
共 16 条
[1]   Keratosis Follicularis Spinulosa Decalvans Is Caused by Mutations in MBTPS2 [J].
Aten, Emmelien ;
Brasz, Lisa C. ;
Bornholdt, Dorothea ;
Hooijkaas, Ingeborg B. ;
Porteous, Mary E. ;
Sybert, Virginia P. ;
Vermeer, Maarten H. ;
Vossen, Rolf H. A. M. ;
van der Wielen, Michiel J. R. ;
Bakker, Egbert ;
Breuning, Martijn H. ;
Grzeschik, Karl-Heinz ;
Oosterwijk, Jan C. ;
den Dunnen, Johan T. .
HUMAN MUTATION, 2010, 31 (10) :1125-1133
[2]   Olmsted syndrome: The clinical spectrum of mutilating palmoplantar keratoderma [J].
Bergonse, FN ;
Rabello, SM ;
Barreto, RL ;
Romiti, R ;
Nico, MMS ;
Aoki, V ;
Reis, VMS ;
Rivitti, EA .
PEDIATRIC DERMATOLOGY, 2003, 20 (04) :323-326
[3]   OLMSTED SYNDROME IN TWINS [J].
CAMBIAGHI, S ;
TADINI, G ;
BARBARESCHI, M ;
CAPUTO, R .
ARCHIVES OF DERMATOLOGY, 1995, 131 (06) :738-739
[4]   A novel mutation in MBTPS2 causes ichthyosis follicularis, alopecia and photophobia (IFAP) syndrome in a Chinese family [J].
Ding, Y. G. ;
Wang, J. Y. ;
Qiao, J. J. ;
Mao, X. H. ;
Cai, S. Q. .
BRITISH JOURNAL OF DERMATOLOGY, 2010, 163 (04) :886-889
[5]  
Larregue M, 2000, J Dermatol, V27, P557
[6]   Exome Sequencing Reveals Mutations in TRPV3 as a Cause of Olmsted Syndrome [J].
Lin, Zhimiao ;
Chen, Quan ;
Lee, Mingyang ;
Cao, Xu ;
Zhang, Jie ;
Ma, Donglai ;
Chen, Long ;
Hu, Xiaoping ;
Wang, Huijun ;
Wang, Xiaowen ;
Zhang, Peng ;
Liu, Xuanzhu ;
Guan, Liping ;
Tang, Yiquan ;
Yang, Haizhen ;
Tu, Ping ;
Bu, Dingfang ;
Zhu, Xuejun ;
Wang, KeWei ;
Li, Ruoyu ;
Yang, Yong .
AMERICAN JOURNAL OF HUMAN GENETICS, 2012, 90 (03) :558-564
[7]   Mutilating palmoplantar keratoderma with periorificial keratotic plaques [J].
Mevorah, B ;
Goldberg, I ;
Sprecher, E ;
Bergman, R ;
Metzker, A ;
Luria, R ;
Gat, A ;
Brenner, S .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2005, 53 (05) :S266-S272
[8]   MBTPS2 Mutation Causes BRESEK/BRESHECK Syndrome [J].
Naiki, Misako ;
Mizuno, Seiji ;
Yamada, Kenichiro ;
Yamada, Yasukazu ;
Kimura, Reiko ;
Oshiro, Makoto ;
Okamoto, Nobuhiko ;
Makita, Yoshio ;
Seishima, Mariko ;
Wakamatsu, Nobuaki .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2012, 158A (01) :97-102
[9]   IFAP Syndrome Is Caused by Deficiency in MBTPS2, an Intramembrane Zinc Metalloprotease Essential for Cholesterol Homeostasis and ER Stress Response [J].
Oeffner, Frank ;
Fischer, Gayle ;
Happle, Rudolf ;
Koenig, Arne ;
Betz, Regina C. ;
Bornholdt, Dorothea ;
Neidel, Ulrike ;
Boente, Maria del Carmen ;
Redler, Silke ;
Romero-Gomez, Javier ;
Salhi, Aicha ;
Vera-Casano, Angel ;
Weirich, Christian ;
Grzeschik, Karl-Heinz .
AMERICAN JOURNAL OF HUMAN GENETICS, 2009, 84 (04) :459-467
[10]   Keratodermia palmaris et plantaris congenitalis - Report of a case showing associated lesions of unusual location [J].
Olmsted, HC .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1927, 33 (05) :757-764