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
  • [31] Radiographical Survey of Osteochondrodysplasia in Scottish Fold Cats caused by the TRPV4 gene variant
    Rorden, Chris
    Griswold, Marilee C.
    Moses, Nan
    Berry, Clifford R.
    Keller, G. Gregory
    Rivas, Rudy
    Flores-Smith, Helen
    Shaffer, Lisa G.
    Malik, Richard
    HUMAN GENETICS, 2021, 140 (11) : 1525 - 1534
  • [32] Radiographical Survey of Osteochondrodysplasia in Scottish Fold Cats caused by the TRPV4 gene variant
    Chris Rorden
    Marilee C. Griswold
    Nan Moses
    Clifford R. Berry
    G. Gregory Keller
    Rudy Rivas
    Helen Flores-Smith
    Lisa G. Shaffer
    Richard Malik
    Human Genetics, 2021, 140 : 1525 - 1534
  • [33] TRPV4 deficiency causes sexual dimorphism in bone metabolism and osteoporotic fracture risk
    van der Eerden, B. C. J.
    Oei, L.
    Roschger, P.
    Fratzl-Zelman, N.
    Hoenderop, J. G. J.
    van Schoor, N. M.
    Pettersson-Kymmer, U.
    Schreuders-Koedam, M.
    Uitterlinden, A. G.
    Hofman, A.
    Suzuki, M.
    Klaushofer, K.
    Ohlsson, C.
    Lips, P. J. A.
    Rivadeneira, F.
    Bindels, R. J. M.
    van Leeuwen, J. P. T. M.
    BONE, 2013, 57 (02) : 443 - 454
  • [34] Novel TRPV4 mutation in a large Chinese family with congenital distal spinal muscular atrophy, skeletal dysplasia and scaly skin
    Liu, Ying
    Yan, Xuejing
    Chen, Yongzhen
    He, Zhiyi
    Ouyang, Yi
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2020, 419
  • [35] Homozygous TRPV4 mutation causes congenital distal spinal muscular atrophy and arthrogryposis
    Velilla, Jose
    Marchetti, Michael Mario
    Toth-Petroczy, Agnes
    Grosgogeat, Claire
    Bennett, Alexis H.
    Carmichael, Nikkola
    Estrella, Elicia
    Darras, Basil T.
    Frank, Natasha Y.
    Krier, Joel
    Gaudet, Rachelle
    Gupta, Vandana A.
    Maas, Richard L.
    Sunyaev, Shamil
    Cassa, Christopher
    Green, Robert
    Goessling, Wolfram
    Haghighi, Alireza
    Fieg, Elizabeth
    MacRae, Calum
    Raychaudhuri, Soumya
    Seidman, Christine
    Patsopolous, Nikolaos
    Soylemez, Onuralp
    NEUROLOGY-GENETICS, 2019, 5 (02)
  • [36] A novel antagonist of TRPM2 and TRPV4 channels: Carvacrol
    Naziroglu, Mustafa
    METABOLIC BRAIN DISEASE, 2022, 37 (03) : 711 - 728
  • [37] A novel antagonist of TRPM2 and TRPV4 channels: Carvacrol
    Mustafa Nazıroğlu
    Metabolic Brain Disease, 2022, 37 : 711 - 728
  • [38] TRPV4 ion channel is a novel regulator of dermal myofibroblast differentiation
    Sharma, Shweta
    Goswami, Rishov
    Merth, Michael
    Cohen, Jonathan
    Lei, Kai Y.
    Zhang, David X.
    Rahaman, Shaik O.
    AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2017, 312 (05): : C562 - C572
  • [39] TRPV2 and TRPV4, potential novel pharmacological targets for endothelial hyperpermeability in the diabetic eye
    Rollo, Adam
    Augustine, Josy
    Barabas, Peter
    Simpson, David
    Curtis, Tim
    BRITISH JOURNAL OF PHARMACOLOGY, 2023, 180 (04) : 521 - 522
  • [40] THE REMARKABLE PHENOTYPIC VARIABILITY OF THE p.Arg269HiS VARIANT IN THE TRPV4 GENE
    Jedrzejowska, Maria
    Debek, Emilia
    Kowalczyk, Bartlomiej
    Halat, Paulina
    Kostera-Pruszczyk, Anna
    Ciara, Elzbieta
    Jezela-Stanek, Aleksandra
    Rydzanicz, Malgorzata
    Gasperowicz, Piotr
    Gos, Monika
    MUSCLE & NERVE, 2019, 59 (01) : 129 - 133