Novel TRPV4 variant causes a severe form of metatropic dysplasia

被引:6
作者
Graversen, Lise [1 ,2 ]
Haagerup, Annette [3 ,4 ]
Andersen, Brian N. [1 ]
Petersen, Karin K. [5 ]
Gjorup, Vibike [6 ]
Gudmundsdottir, Gudrun [7 ]
Vogel, Ida [2 ]
Gregersen, Pernille A. [1 ,2 ]
机构
[1] Aarhus Univ Hosp, Ctr Rare Dis, Pediat & Adolescent Med, Aarhus, Denmark
[2] Aarhus Univ Hosp, Dept Clin Genet, Aarhus, Denmark
[3] West Danish Hosp, NIDO Danmark, Herning, Denmark
[4] Aarhus Univ, Inst Clin Med, Aarhus, Denmark
[5] Aarhus Univ Hosp, Dept Radiol, Aarhus, Denmark
[6] Aarhus Univ Hosp, Dept Gynaecol & Obstet, Aarhus, Denmark
[7] Aarhus Univ Hosp, Dept Neurosurg, Aarhus, Denmark
关键词
genetic diseases; metatropic dysplasia; rare diseases; TRPV4;
D O I
10.1002/ccr3.1598
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Key Clinical Message We present a girl born with a frontal bossing, short neck, bell-shaped thorax, short limbs with prominent joints, and a tail-like coccygeal appendage. Genetic screening of TRPV4 identified a novel de novo heterozygous missense variant. We believe the variant causes the severe form of metatropic dysplasia in this patient.
引用
收藏
页码:1774 / 1778
页数:5
相关论文
共 14 条
[1]   TRPV4 related skeletal dysplasias: a phenotypic spectrum highlighted byclinical, radiographic, and molecular studies in 21 new families [J].
Andreucci, Elena ;
Aftimos, Salim ;
Alcausin, Melanie ;
Haan, Eric ;
Hunter, Warwick ;
Kannu, Peter ;
Kerr, Bronwyn ;
McGillivray, George ;
Gardner, R. J. McKinlay ;
Patricelli, Maria G. ;
Sillence, David ;
Thompson, Elizabeth ;
Zacharin, Margaret ;
Zankl, Andreas ;
Lamande, Shireen R. ;
Savarirayan, Ravi .
ORPHANET JOURNAL OF RARE DISEASES, 2011, 6
[2]   Dominant TRPV4 Mutations in Nonlethal and Lethal Metatropic Dysplasia [J].
Camacho, Natalia ;
Krakow, Deborah ;
Johnykutty, Sharlin ;
Katzman, Philip J. ;
Pepkowitz, Samuel ;
Vriens, Joris ;
Nilius, Bernd ;
Boyce, Brendan F. ;
Cohn, Daniel H. .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2010, 152A (05) :1169-1177
[3]   TRPV4-Pathy Manifesting Both Skeletal Dysplasia and Peripheral Neuropathy: A Report of Three Patients [J].
Cho, Tae-Joon ;
Matsumoto, Kazu ;
Fano, Virginia ;
Dai, Jin ;
Kim, Ok-Hwa ;
Chae, Jong Hee ;
Yoo, Won Joon ;
Tanaka, Yuji ;
Matsui, Yoshito ;
Takigami, Iori ;
Monges, Soledad ;
Zabel, Bernhard ;
Shimizu, Katsuji ;
Nishimura, Gen ;
Lausch, Ekkehart ;
Ikegawa, Shiro .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2012, 158A (04) :795-802
[4]   Novel and recurrent TRPV4 mutations and their association with distinct phenotypes within the TRPV4 dysplasia family [J].
Dai, J. ;
Kim, O-H ;
Cho, T-J ;
Schmidt-Rimpler, M. ;
Tonoki, H. ;
Takikawa, K. ;
Haga, N. ;
Miyoshi, K. ;
Kitoh, H. ;
Yoo, W-J ;
Choi, I-H ;
Song, H-R ;
Jin, D-K ;
Kim, H-T ;
Kamasaki, H. ;
Bianchi, P. ;
Grigelioniene, G. ;
Nampoothiri, S. ;
Minagawa, M. ;
Miyagawa, S-i ;
Fukao, T. ;
Marcelis, C. ;
Jansweijer, M. C. E. ;
Hennekam, R. C. M. ;
Bedeschi, F. ;
Mustonen, A. ;
Jiang, Q. ;
Ohashi, H. ;
Furuichi, T. ;
Unger, S. ;
Zabel, B. ;
Lausch, E. ;
Superti-Furga, A. ;
Nishimura, G. ;
Ikegawa, S. .
JOURNAL OF MEDICAL GENETICS, 2010, 47 (10) :704-709
[5]   TRPV4-pathy, a novel channelopathy affecting diverse systems [J].
Dai, Jin ;
Cho, Tae-Joon ;
Unger, Sheila ;
Lausch, Ekkehart ;
Nishimura, Gen ;
Kim, Ok-Hwa ;
Superti-Furga, Andrea ;
Ikegawa, Shiro .
JOURNAL OF HUMAN GENETICS, 2010, 55 (07) :400-402
[6]   Scapuloperoneal spinal muscular atrophy and CMT2C are allelic disorders caused by alterations in TRPV4 [J].
Deng, Han-Xiang ;
Klein, Christopher J. ;
Yan, Jianhua ;
Shi, Yong ;
Wu, Yanhong ;
Fecto, Faisal ;
Yau, Hau-Jie ;
Yang, Yi ;
Zhai, Hong ;
Siddique, Nailah ;
Hedley-Whyte, E. Tessa ;
DeLong, Robert ;
Martina, Marco ;
Dyck, Peter J. ;
Siddique, Teepu .
NATURE GENETICS, 2010, 42 (02) :165-U102
[7]   The vanilloid transient receptor potential channel TRPV4: From structure to disease [J].
Everaerts, Wouter ;
Nilius, Bernd ;
Owsianik, Grzegorz .
PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY, 2010, 103 (01) :2-17
[8]   Human skeletal dysplasia caused by a constitutive activated transient receptor potential vanilloid 4 (TRPV4) cation channel mutation [J].
Kang, Sang Sun ;
Shin, Sung Hwa ;
Auh, Chung-Kyoon ;
Chun, Jaesun .
EXPERIMENTAL AND MOLECULAR MEDICINE, 2012, 44 (12) :707-722
[9]   Abnormal osmotic regulation in trpv4-/- mice [J].
Liedtke, W ;
Friedman, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (23) :13698-13703
[10]   Spondylo-Epiphyseal Dysplasia, Maroteaux Type (Pseudo-Morquio Syndrome Type 2), and Parastremmatic Dysplasia are Caused by TRPV4 Mutations [J].
Nishimura, Gen ;
Dai, Jin ;
Lausch, Ekkehart ;
Unger, Sheila ;
Megarbane, Andre ;
Kitoh, Hiroshi ;
Kim, Ok Hwa ;
Cho, Tae-Joon ;
Bedeschi, Francesca ;
Benedicenti, Francesco ;
Mendoza-Londono, Roberto ;
Silengo, Margherita ;
Schmidt-Rimpler, Maren ;
Spranger, Jurgen ;
Zabel, Bernhard ;
Ikegawa, Shiro ;
Superti-Furga, Andrea .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2010, 152A (06) :1443-1449