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
来源
CLINICAL CASE REPORTS | 2018年 / 6卷 / 09期
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 50 条
  • [41] Novel mutation of TRPV4 in congenital distal SMA with vocal cord paralysis
    Fiorillo, C.
    Moro, F.
    Astrea, G.
    Battini, R.
    Gully, C.
    Olschewski, A.
    Auer-Grumbach, M.
    Bruno, C.
    Santorelli, F. M.
    NEUROMUSCULAR DISORDERS, 2011, 21 (9-10) : 682 - 682
  • [42] Discovery and pharmacological characterization of a novel benzimidazole TRPV4 antagonist with cyanocyclobutyl moiety
    Ai, Chongyi
    Wang, Zhuang
    Li, Pengyun
    Wang, Mengyuan
    Zhang, Wenjuan
    Song, Huijuan
    Cai, Xu
    Lv, Kai
    Chen, Xingjuan
    Zheng, Zhibing
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2023, 249
  • [43] A novel potent TRPV4 associated protein participates in endochondral bone formation
    Mizuno, Atsuko
    Suzuki, Makoto
    Taniguchi, Junichi
    Koshimizu, Taka-aki
    JOURNAL OF PHARMACOLOGICAL SCIENCES, 2009, 109 : 176P - 176P
  • [44] Prenatal diagnosis of a de novo TRPV4 associated skeletal dysplasia by targeted next generation sequencing
    Daumer-Haas, C.
    Shoukier, M.
    Bagowski, C. P.
    Liebrecht, D.
    Minderer, S.
    Gloning, K. P.
    Schramm, T.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2018, 26 : 252 - 253
  • [45] Increased Basal Activity Is a Key Determinant in the Severity of Human Skeletal Dysplasia Caused by TRPV4 Mutations
    Loukin, Stephen
    Su, Zhenwei
    Kung, Ching
    PLOS ONE, 2011, 6 (05):
  • [46] HETEROGENEITY OF SPONASTRIME DYSPLASIA - DELINEATION OF A VARIANT FORM WITH SEVERE MENTAL-RETARDATION
    VERLOES, A
    MISSON, JP
    DUBRU, JM
    JAMBLIN, P
    LEMERRER, M
    CLINICAL DYSMORPHOLOGY, 1995, 4 (03) : 208 - 215
  • [47] Novel filamin C (FLNC) variant causes a severe form of familial mixed hypertrophic-restrictive cardiomyopathy
    Gaudreault, Nathalie
    Ruel, Louis-Jacques
    Henry, Cyndi
    Schleit, Jennifer
    Laguee, Patrick
    Champagne, Jean
    Senechal, Mario
    Sarrazin, Jean-Francois
    Philippon, Francois
    Bosse, Yohan
    Steinberg, Christian
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2023, 191 (06) : 1508 - 1517
  • [48] TRPV4 mutations causing mixed neuropathy and skeletal phenotypes result in severe gain of function
    Taga, Arens
    Peyton, Margo A.
    Goretzki, Benedikt
    Gallagher, Thomas Q.
    Ritter, Ann
    Harper, Amy
    Crawford, Thomas O.
    Hellmich, Ute A.
    Sumner, Charlotte J.
    McCray, Brett A.
    ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY, 2022, 9 (03): : 375 - +
  • [49] Cathepsin S Causes Inflammatory Pain via Biased Agonism of PAR2 and TRPV4
    Zhao, Peishen
    Lieu, TinaMarie
    Barlow, Nicholas
    Metcalf, Matthew
    Veldhuis, Nicholas A.
    Jensen, Dane D.
    Kocan, Martina
    Sostegni, Silvia
    Haerteis, Silke
    Baraznenok, Vera
    Henderson, Ian
    Lindstrom, Erik
    Guerrero-Alba, Raquel
    Valdez-Morales, Eduardo E.
    Liedtke, Wolfgang
    McIntyre, Peter
    Vanner, Stephen J.
    Korbmacher, Christoph
    Bunnett, Nigel W.
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2014, 289 (39) : 27215 - 27234
  • [50] A Novel CEBPE Variant Causes Severe Infections and Profound Neutropenia
    Banday, Aaqib Zaffar
    Kaur, Anit
    Akagi, Tadayuki
    Bhattarai, Dharmagat
    Muraoka, Masahiro
    Dev, Diksha
    Das, Jhumki
    Sachdeva, Man Updesh Singh
    Karmakar, Indrani
    Arora, Kanika
    Kaur, Gurjit
    Pandiarajan, Vignesh
    Jindal, Ankur Kumar
    Wada, Taizo
    Koeffler, H. Phillip
    Suri, Deepti
    Ahluwalia, Jasmina
    Kanegane, Hirokazu
    Bhatia, Prateek
    Rawat, Amit
    Singh, Surjit
    JOURNAL OF CLINICAL IMMUNOLOGY, 2022, 42 (07) : 1434 - 1450