Literature DB >> 27888646

Corner fracture type spondylometaphyseal dysplasia: Overlap with type II collagenopathies.

Keren Machol1, Mahim Jain1, Mohammed Almannai1, Thibault Orand1, James T Lu1,2, Alyssa Tran1, Yuqing Chen1, Alan Schlesinger3, Richard Gibbs1,2, Luisa Bonafe4, Ana Belinda Campos-Xavier4, Sheila Unger5, Andrea Superti-Furga5, Brendan H Lee1, Philippe M Campeau6, Lindsay C Burrage1.   

Abstract

Spondylometaphyseal dysplasia (SMD) corner fracture type (also known as SMD "Sutcliffe" type, MIM 184255) is a rare skeletal dysplasia that presents with mild to moderate short stature, developmental coxa vara, mild platyspondyly, corner fracture-like lesions, and metaphyseal abnormalities with sparing of the epiphyses. The molecular basis for this disorder has yet to be clarified. We describe two patients with SMD corner fracture type and heterozygous pathogenic variants in COL2A1. These two cases together with a third case of SMD corner fracture type with a heterozygous COL2A1 pathogenic variant previously described suggest that this disorder overlaps with type II collagenopathies. The finding of one of the pathogenic variants in a previously reported case of spondyloepimetaphyseal dysplasia (SEMD) Strudwick type and the significant clinical similarity suggest an overlap between SMD corner fracture and SEMD Strudwick types.
© 2016 Wiley Periodicals, Inc. © 2016 Wiley Periodicals, Inc.

Entities:  

Keywords:  COL2A1; Sutcliffe type; corner fracture; developmental coxa vara; skeletal dysplasia; spondylometaphyseal dysplasia

Mesh:

Substances:

Year:  2016        PMID: 27888646      PMCID: PMC5315610          DOI: 10.1002/ajmg.a.38059

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  23 in total

1.  A pilot study of gene testing of genetic bone dysplasia using targeted next-generation sequencing.

Authors:  Huiwen Zhang; Rui Yang; Yu Wang; Jun Ye; Lianshu Han; Wenjuan Qiu; Xuefan Gu
Journal:  J Hum Genet       Date:  2015-09-17       Impact factor: 3.172

2.  The Shwachman-Bodian-Diamond syndrome gene mutations cause a neonatal form of spondylometaphysial dysplasia (SMD) resembling SMD Sedaghatian type.

Authors:  Gen Nishimura; Eiji Nakashima; Yuichiro Hirose; Trevor Cole; Phillip Cox; Daniel H Cohn; David L Rimoin; Ralph S Lachman; Yoshinari Miyamoto; Bronwyn Kerr; Sheila Unger; Hirofumi Ohashi; Andrea Superti-Furga; Shiro Ikegawa
Journal:  J Med Genet       Date:  2007-04       Impact factor: 6.318

3.  Genetic deficiency of tartrate-resistant acid phosphatase associated with skeletal dysplasia, cerebral calcifications and autoimmunity.

Authors:  Ekkehart Lausch; Andreas Janecke; Matthias Bros; Stefanie Trojandt; Yasemin Alanay; Corinne De Laet; Christian A Hübner; Peter Meinecke; Gen Nishimura; Mari Matsuo; Yoshiko Hirano; Sylvie Tenoutasse; Andrea Kiss; Rafael Fabiano Machado Rosa; Sharon L Unger; Raffaele Renella; Luisa Bonafé; Jürgen Spranger; Sheila Unger; Bernhard Zabel; Andrea Superti-Furga
Journal:  Nat Genet       Date:  2011-01-09       Impact factor: 38.330

4.  A study of the clinical and radiological features in a cohort of 93 patients with a COL2A1 mutation causing spondyloepiphyseal dysplasia congenita or a related phenotype.

Authors:  Paulien A Terhal; Rutger Jan A J Nievelstein; Eva J J Verver; Vedat Topsakal; Paula van Dommelen; Kristien Hoornaert; Martine Le Merrer; Andreas Zankl; Marleen E H Simon; Sarah F Smithson; Carlo Marcelis; Bronwyn Kerr; Jill Clayton-Smith; Esther Kinning; Sahar Mansour; Frances Elmslie; Linda Goodwin; Annemarie H van der Hout; Hermine E Veenstra-Knol; Johanna C Herkert; Allan M Lund; Raoul C M Hennekam; André Mégarbané; Melissa M Lees; Louise C Wilson; Alison Male; Jane Hurst; Yasemin Alanay; Göran Annerén; Regina C Betz; Ernie M H F Bongers; Valerie Cormier-Daire; Anne Dieux; Albert David; Mariet W Elting; Jenneke van den Ende; Andrew Green; Johanna M van Hagen; Niels Thomas Hertel; Muriel Holder-Espinasse; Nicolette den Hollander; Tessa Homfray; Hanne D Hove; Susan Price; Annick Raas-Rothschild; Marianne Rohrbach; Barbara Schroeter; Mohnish Suri; Elizabeth M Thompson; Edward S Tobias; Annick Toutain; Maaike Vreeburg; Emma Wakeling; Nine V Knoers; Paul Coucke; Geert R Mortier
Journal:  Am J Med Genet A       Date:  2015-01-21       Impact factor: 2.802

5.  Spondylometaphyseal dysplasia, corner fracture type: a heritable condition associated with coxa vara.

Authors:  L O Langer; P W Brill; M B Ozonoff; R M Pauli; W G Wilson; B A Alford; H Pavlov; D G Drake
Journal:  Radiology       Date:  1990-06       Impact factor: 11.105

6.  Dominant mutations in the type II collagen gene, COL2A1, produce spondyloepimetaphyseal dysplasia, Strudwick type.

Authors:  G E Tiller; P A Polumbo; M A Weis; R Bogaert; R S Lachman; D H Cohn; D L Rimoin; D R Eyre
Journal:  Nat Genet       Date:  1995-09       Impact factor: 38.330

Review 7.  Mutation Update for COL2A1 Gene Variants Associated with Type II Collagenopathies.

Authors:  Mouna Barat-Houari; Guillaume Sarrabay; Vincent Gatinois; Aurélie Fabre; Bruno Dumont; David Genevieve; Isabelle Touitou
Journal:  Hum Mutat       Date:  2015-10-21       Impact factor: 4.878

8.  Mutations in PCYT1A, encoding a key regulator of phosphatidylcholine metabolism, cause spondylometaphyseal dysplasia with cone-rod dystrophy.

Authors:  Julie Hoover-Fong; Nara Sobreira; Julie Jurgens; Peggy Modaff; Carrie Blout; Ann Moser; Ok-Hwa Kim; Tae-Joon Cho; Sung Yoon Cho; Sang Jin Kim; Dong-Kyu Jin; Hiroshi Kitoh; Woong-Yang Park; Hua Ling; Kurt N Hetrick; Kimberly F Doheny; David Valle; Richard M Pauli
Journal:  Am J Hum Genet       Date:  2014-01-02       Impact factor: 11.025

9.  Identifying non-accidental fractures in children aged <2 years.

Authors:  Laura A Leaman; William L Hennrikus; James J Bresnahan
Journal:  J Child Orthop       Date:  2016-06-23       Impact factor: 1.548

10.  Axial Spondylometaphyseal Dysplasia Is Caused by C21orf2 Mutations.

Authors:  Zheng Wang; Aritoshi Iida; Noriko Miyake; Koji M Nishiguchi; Kosuke Fujita; Toru Nakazawa; Abdulrahman Alswaid; Mohammed A Albalwi; Ok-Hwa Kim; Tae-Joon Cho; Gye-Yeon Lim; Bertrand Isidor; Albert David; Cecilie F Rustad; Else Merckoll; Jostein Westvik; Eva-Lena Stattin; Giedre Grigelioniene; Ikuyo Kou; Masahiro Nakajima; Hirohumi Ohashi; Sarah Smithson; Naomichi Matsumoto; Gen Nishimura; Shiro Ikegawa
Journal:  PLoS One       Date:  2016-03-14       Impact factor: 3.240

View more
  2 in total

1.  Mechanistic insights into the cellular effects of a novel FN1 variant associated with a spondylometaphyseal dysplasia.

Authors:  E B Cadoff; R Sheffer; S Wientroub; D Ovadia; V Meiner; J E Schwarzbauer
Journal:  Clin Genet       Date:  2018-09-03       Impact factor: 4.438

2.  Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with "Corner Fractures".

Authors:  Chae Syng Lee; He Fu; Nissan Baratang; Justine Rousseau; Heena Kumra; V Reid Sutton; Marcello Niceta; Andrea Ciolfi; Guilherme Yamamoto; Débora Bertola; Carlo L Marcelis; Dorien Lugtenberg; Andrea Bartuli; Choel Kim; Julie Hoover-Fong; Nara Sobreira; Richard Pauli; Carlos Bacino; Deborah Krakow; Jillian Parboosingh; Patrick Yap; Ariana Kariminejad; Marie T McDonald; Mariana I Aracena; Ekkehart Lausch; Sheila Unger; Andrea Superti-Furga; James T Lu; Dan H Cohn; Marco Tartaglia; Brendan H Lee; Dieter P Reinhardt; Philippe M Campeau
Journal:  Am J Hum Genet       Date:  2017-11-02       Impact factor: 11.025

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.