Literature DB >> 21863289

The importance of conventional radiography in the mutational analysis of skeletal dysplasias (the TRPV4 mutational family).

Stefan F Nemec1, Daniel H Cohn, Deborah Krakow, Vincent A Funari, David L Rimoin, Ralph S Lachman.   

Abstract

The spondylo and spondylometaphyseal dysplasias (SMDs) are characterized by vertebral changes and metaphyseal abnormalities of the tubular bones, which produce a phenotypic spectrum of disorders from the mild autosomal-dominant brachyolmia to SMD Kozlowski to autosomal-dominant metatropic dysplasia. Investigations have recently drawn on the similar radiographic features of those conditions to define a new family of skeletal dysplasias caused by mutations in the transient receptor potential cation channel vanilloid 4 (TRPV4). This review demonstrates the significance of radiography in the discovery of a new bone dysplasia family due to mutations in a single gene.

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Year:  2011        PMID: 21863289     DOI: 10.1007/s00247-011-2229-6

Source DB:  PubMed          Journal:  Pediatr Radiol        ISSN: 0301-0449


  25 in total

Review 1.  Collagen, genes and the skeletal dysplasias on the edge of a new era: a review and update.

Authors:  R S Lachman; G E Tiller; J M Graham; D L Rimoin
Journal:  Eur J Radiol       Date:  1992 Jan-Feb       Impact factor: 3.528

Review 2.  A family of chondrodysplasias caused by mutations in the diastrophic dysplasia sulfate transporter gene and associated with impaired sulfation of proteoglycans.

Authors:  A Superti-Furga; J Hästbacka; A Rossi; J J van der Harten; W R Wilcox; D H Cohn; D L Rimoin; B Steinmann; E S Lander; R Gitzelmann
Journal:  Ann N Y Acad Sci       Date:  1996-06-08       Impact factor: 5.691

3.  Excretion of chondroitin sulfate C with low sulfate content by patients with generalized platyspondyly (brachyolmia).

Authors:  P A Mour ao; S P Toledo; H B Nader; C P Dietrich
Journal:  Biochem Med       Date:  1973-06

Review 4.  Transient receptor potential vanilloid 4: The sixth sense of the musculoskeletal system?

Authors:  Farshid Guilak; Holly A Leddy; Wolfgang Liedtke
Journal:  Ann N Y Acad Sci       Date:  2010-03       Impact factor: 5.691

Review 5.  Revisiting metatropic dysplasia: presentation of a series of 19 novel patients and review of the literature.

Authors:  D Geneviève; M Le Merrer; J Feingold; A Munnich; P Maroteaux; V Cormier-Daire
Journal:  Am J Med Genet A       Date:  2008-04-15       Impact factor: 2.802

6.  Atelosteogenesis type II is caused by mutations in the diastrophic dysplasia sulfate-transporter gene (DTDST): evidence for a phenotypic series involving three chondrodysplasias.

Authors:  J Hästbacka; A Superti-Furga; W R Wilcox; D L Rimoin; D H Cohn; E S Lander
Journal:  Am J Hum Genet       Date:  1996-02       Impact factor: 11.025

7.  Mutations in the gene encoding filamin B disrupt vertebral segmentation, joint formation and skeletogenesis.

Authors:  Deborah Krakow; Stephen P Robertson; Lily M King; Timothy Morgan; Eiman T Sebald; Cristina Bertolotto; Sebastian Wachsmann-Hogiu; Dora Acuna; Sandor S Shapiro; Toshiro Takafuta; Salim Aftimos; Chong Ae Kim; Helen Firth; Carlos E Steiner; Valerie Cormier-Daire; Andrea Superti-Furga; Luisa Bonafe; John M Graham; Arthur Grix; Carlos A Bacino; Judith Allanson; Martin G Bialer; Ralph S Lachman; David L Rimoin; Daniel H Cohn
Journal:  Nat Genet       Date:  2004-02-29       Impact factor: 38.330

8.  Broad phenotypic spectrum caused by an identical heterozygous CDMP-1 mutation in three unrelated families.

Authors:  Ravi Savarirayan; Susan M White; Frances R Goodman; John M Graham; Martin B Delatycki; Ralph S Lachman; David L Rimoin; David B Everman; Matthew L Warman
Journal:  Am J Med Genet A       Date:  2003-03-01       Impact factor: 2.802

9.  Alterations in the ankyrin domain of TRPV4 cause congenital distal SMA, scapuloperoneal SMA and HMSN2C.

Authors:  Michaela Auer-Grumbach; Andrea Olschewski; Lea Papić; Hannie Kremer; Meriel E McEntagart; Sabine Uhrig; Carina Fischer; Eleonore Fröhlich; Zoltán Bálint; Bi Tang; Heimo Strohmaier; Hanns Lochmüller; Beate Schlotter-Weigel; Jan Senderek; Angelika Krebs; Katherine J Dick; Richard Petty; Cheryl Longman; Neil E Anderson; George W Padberg; Helenius J Schelhaas; Conny M A van Ravenswaaij-Arts; Thomas R Pieber; Andrew H Crosby; Christian Guelly
Journal:  Nat Genet       Date:  2009-12-27       Impact factor: 38.330

Review 10.  Nosology and classification of genetic skeletal disorders: 2010 revision.

Authors:  Matthew L Warman; Valerie Cormier-Daire; Christine Hall; Deborah Krakow; Ralph Lachman; Martine LeMerrer; Geert Mortier; Stefan Mundlos; Gen Nishimura; David L Rimoin; Stephen Robertson; Ravi Savarirayan; David Sillence; Juergen Spranger; Sheila Unger; Bernhard Zabel; Andrea Superti-Furga
Journal:  Am J Med Genet A       Date:  2011-03-15       Impact factor: 2.802

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  6 in total

1.  SMD Kozlowski type caused by p.Arg594His substitution in TRPV4 reveals abnormal ossification and notochordal remnants in discs and vertebrae.

Authors:  Tadeusz Bieganski; Peter Beighton; Maciej Lukaszewski; Krzysztof Bik; Lukasz Kuszel; Ewa Wasilewska; Kazimierz Kozlowski; Malwina Czarny-Ratajczak
Journal:  Eur J Med Genet       Date:  2017-07-04       Impact factor: 2.708

2.  Autosomal dominant brachyolmia: transient metaphyseal striations.

Authors:  Yun-Jung Lim; Hye-Ran Lee; Ok-Hwa Kim; Tae-Joon Cho; Kun-Bo Park
Journal:  Skeletal Radiol       Date:  2017-06-10       Impact factor: 2.199

Review 3.  Human skeletal dysplasia caused by a constitutive activated transient receptor potential vanilloid 4 (TRPV4) cation channel mutation.

Authors:  Sang Sun Kang; Sung Hwa Shin; Chung-Kyoon Auh; Jaesun Chun
Journal:  Exp Mol Med       Date:  2012-12-31       Impact factor: 8.718

4.  Spondylometaphyseal dysplasia: an uncommon disease.

Authors:  Márcio Luís Duarte; Élcio Roberto Duarte; Daniela Brasil Solorzano; Edgar Brasil Solorzano; Jael Brasil de Alcântara Ferreira
Journal:  Radiol Bras       Date:  2017 Jan-Feb

Review 5.  TRPing to the Point of Clarity: Understanding the Function of the Complex TRPV4 Ion Channel.

Authors:  Trine L Toft-Bertelsen; Nanna MacAulay
Journal:  Cells       Date:  2021-01-15       Impact factor: 6.600

6.  TRPV4 mutations causing mixed neuropathy and skeletal phenotypes result in severe gain of function.

Authors:  Arens Taga; Margo A Peyton; Benedikt Goretzki; Thomas Q Gallagher; Ann Ritter; Amy Harper; Thomas O Crawford; Ute A Hellmich; Charlotte J Sumner; Brett A McCray
Journal:  Ann Clin Transl Neurol       Date:  2022-02-16       Impact factor: 4.511

  6 in total

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