No mutation of elastin and fibulin-5 genes in a patient with acquired cutis laxa associated with chronic urticaria

被引：3
|
作者：
Sun, X. -K. [1 ]
Chen, J. -F. [1 ]
机构：
[1] Third Peoples Hosp Hangzhou, Dept Dermatol, Hangzhou 310009, Zhejiang, Peoples R China
来源：
BRITISH JOURNAL OF DERMATOLOGY | 2011年 / 164卷 / 01期
关键词：
MYELOMA;
D O I：
10.1111/j.1365-2133.2010.10049.x
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：215 / 217
页数：3
相关论文
共 19 条
  • [1] Inflammatory destruction of elastic fibers in acquired cutis laxa is associated with missense alleles in the elastin and fibulin-5 genes
    Hu, Qirui
    Reymond, Jean-Louis
    Pinel, Nicole
    Zabot, Marie-Therese
    Urban, Zsolt
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2006, 126 (02) : 283 - 290
  • [2] Mutation of the fibulin-5 gene in recessive autosomal cutis laxa
    Dereure, O
    ANNALES DE DERMATOLOGIE ET DE VENEREOLOGIE, 2004, 131 (05): : 516 - 516
  • [3] ACQUIRED CUTIS LAXA ASSOCIATED WITH CHRONIC URTICARIA
    CHUN, SI
    YOON, J
    JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1995, 33 (05) : 896 - 899
  • [4] Fibulin-5 mutations in recessive cutis laxa
    Hu, Q.
    Coucke, P. J.
    Sommer, P.
    Davis, E. C.
    Reinhardt, D. P.
    Mecham, R. P.
    Urban, Z.
    MATRIX BIOLOGY, 2006, 25 : S16 - S17
  • [5] Inflammatory destruction of elastic fibers in acquired cutis laxa is associated with missense alleles in the elastin and fibulin-5 genes (vol 126, pg 283, 2006)
    Hu
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2006, 126 (06) : 1426 - 1426
  • [6] Homozygous missense mutation in fibulin-5 in an Iranian autosomal recessive cutis laxa pedigree and associated haplotype
    Elahi, Elahe
    Kalhor, Reza
    Banihosseini, Setareh S.
    Torabi, Noorossadat
    Pour-Jafari, Hamid
    Houshmand, Massoud
    Amini, Seyed S. H.
    Ramezani, Ahmad
    Loeys, Bart
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2006, 126 (07) : 1506 - 1509
  • [7] Homozygosity for a missense mutation in fibulin-5 (FBLN5) results in a severe form of cutis laxa
    Loeys, B
    Van Maldergem, L
    Mortier, G
    Coucke, P
    Gerniers, S
    Naeyaert, JM
    De Paepe, A
    HUMAN MOLECULAR GENETICS, 2002, 11 (18) : 2113 - 2118
  • [8] Homozygosity for a missense mutation in fibulin-5 (FBLN5) results in a severe form of cutis laxa.
    Loeys, B
    Van Maldergem, L
    Mortier, G
    Coucke, P
    Gerniers, S
    Naeyaert, JM
    De Paepe, A
    AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 210 - 210
  • [9] A Novel Elastin Gene Mutation in a Vietnamese Patient with Cutis Laxa
    Siefring, Mark L.
    Lawrence, Elizabeth C.
    Nguyen, Tom C.
    Doanh Lu
    Giang Pham
    Lorenchick, Christa
    Levine, Kara L.
    Urban, Zsolt
    PEDIATRIC DERMATOLOGY, 2014, 31 (03) : 347 - 349
  • [10] Fibulin-5 mutations: mechanisms of impaired elastic fiber formation in recessive cutis laxa
    Hu, Qirui
    Loeys, Bart L.
    Coucke, Paul J.
    De Paepe, Anne
    Mecham, Robert P.
    Choi, Jiwon
    Davis, Elaine C.
    Urban, Zsolt
    HUMAN MOLECULAR GENETICS, 2006, 15 (23) : 3379 - 3386
12