Literature DB >> 16670815

Genetic analysis of skeletal dysplasia: recent advances and perspectives in the post-genome-sequence era.

Shiro Ikegawa1.   

Abstract

Skeletal dysplasia is a group of disorders of the skeleton that result from derangement of growth, development and/or differentiation of the skeleton. Nearly 300 disorders are included; most of them are monogenic diseases. Responsible genes for skeletal dysplasia have been identified in more than 150 diseases mainly through positional cloning. Identification of disease genes would improve patient care through genetic diagnosis as well as improving our understanding of the diseases and molecular mechanism of skeletal tissue formation. Studies of skeletal dysplasia would also help identify disease genes for common diseases affecting bones and joints. In this study, the author reviews recent advances and the current status of the genetic analysis of skeletal dysplasia and its impacts on research into skeletal biology.

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Year:  2006        PMID: 16670815     DOI: 10.1007/s10038-006-0401-x

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  44 in total

1.  Tandem duplication within a type II collagen gene (COL2A1) exon in an individual with spondyloepiphyseal dysplasia.

Authors:  G E Tiller; D L Rimoin; L W Murray; D H Cohn
Journal:  Proc Natl Acad Sci U S A       Date:  1990-05       Impact factor: 11.205

2.  Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development.

Authors:  F Otto; A P Thornell; T Crompton; A Denzel; K C Gilmour; I R Rosewell; G W Stamp; R S Beddington; S Mundlos; B R Olsen; P B Selby; M J Owen
Journal:  Cell       Date:  1997-05-30       Impact factor: 41.582

3.  COL9A3: A third locus for multiple epiphyseal dysplasia.

Authors:  P Paassilta; J Lohiniva; S Annunen; J Bonaventure; M Le Merrer; L Pai; L Ala-Kokko
Journal:  Am J Hum Genet       Date:  1999-04       Impact factor: 11.025

4.  Mutation of the type X collagen gene (COL10A1) causes spondylometaphyseal dysplasia.

Authors:  S Ikegawa; G Nishimura; T Nagai; T Hasegawa; H Ohashi; Y Nakamura
Journal:  Am J Hum Genet       Date:  1998-12       Impact factor: 11.025

5.  Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene.

Authors:  J W Foster; M A Dominguez-Steglich; S Guioli; C Kwok; P A Weller; M Stevanović; J Weissenbach; S Mansour; I D Young; P N Goodfellow
Journal:  Nature       Date:  1994-12-08       Impact factor: 49.962

6.  A type X collagen mutation causes Schmid metaphyseal chondrodysplasia.

Authors:  M L Warman; M Abbott; S S Apte; T Hefferon; I McIntosh; D H Cohn; J T Hecht; B R Olsen; C A Francomano
Journal:  Nat Genet       Date:  1993-09       Impact factor: 38.330

7.  Novel and recurrent mutations clustered in the von Willebrand factor A domain of MATN3 in multiple epiphyseal dysplasia.

Authors:  Akihiko Mabuchi; Nobuhiko Haga; Koichi Maeda; Eiji Nakashima; Noriyo Manabe; Hisatada Hiraoka; Hiroshi Kitoh; Rika Kosaki; Gen Nishimura; Hirofumi Ohashi; Shiro Ikegawa
Journal:  Hum Mutat       Date:  2004-11       Impact factor: 4.878

8.  Achondroplasia is defined by recurrent G380R mutations of FGFR3.

Authors:  G A Bellus; T W Hefferon; R I Ortiz de Luna; J T Hecht; W A Horton; M Machado; I Kaitila; I McIntosh; C A Francomano
Journal:  Am J Hum Genet       Date:  1995-02       Impact factor: 11.025

9.  Novel and recurrent COMP (cartilage oligomeric matrix protein) mutations in pseudoachondroplasia and multiple epiphyseal dysplasia.

Authors:  S Ikegawa; H Ohashi; G Nishimura; K C Kim; A Sannohe; M Kimizuka; Y Fukushima; T Nagai; Y Nakamura
Journal:  Hum Genet       Date:  1998-12       Impact factor: 4.132

10.  Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3.

Authors:  P L Tavormina; R Shiang; L M Thompson; Y Z Zhu; D J Wilkin; R S Lachman; W R Wilcox; D L Rimoin; D H Cohn; J J Wasmuth
Journal:  Nat Genet       Date:  1995-03       Impact factor: 38.330

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  9 in total

1.  Pseudoachondroplasia and the seven Ovitz siblings who survived Auschwitz.

Authors:  Oliver J Muensterer; Walter E Berdon; Ralph S Lachman; Stephen L Done
Journal:  Pediatr Radiol       Date:  2012-03-18

Review 2.  Synovial joints: from development to homeostasis.

Authors:  Lara Longobardi; Tieshi Li; Lidia Tagliafierro; Joseph D Temple; Helen H Willcockson; Ping Ye; Alessandra Esposito; Fuhua Xu; Anna Spagnoli
Journal:  Curr Osteoporos Rep       Date:  2015-02       Impact factor: 5.096

3.  Synovial joint morphogenesis requires the chondrogenic action of Sox5 and Sox6 in growth plate and articular cartilage.

Authors:  Peter Dy; Patrick Smits; Amber Silvester; Alfredo Penzo-Méndez; Bogdan Dumitriu; Yu Han; Carol A de la Motte; David M Kingsley; Véronique Lefebvre
Journal:  Dev Biol       Date:  2010-03-04       Impact factor: 3.582

Review 4.  Vertebrate skeletogenesis.

Authors:  Véronique Lefebvre; Pallavi Bhattaram
Journal:  Curr Top Dev Biol       Date:  2010       Impact factor: 4.897

Review 5.  Windswept Deformity a Disease or a Symptom? A Systematic Review on the Aetiologies and Hypotheses of Simultaneous Genu Valgum and Varum in Children.

Authors:  Niels J Jansen; Romy B M Dockx; Adhiambo M Witlox; Saartje Straetemans; Heleen M Staal
Journal:  Children (Basel)       Date:  2022-05-10

6.  SOXC Transcription Factors Induce Cartilage Growth Plate Formation in Mouse Embryos by Promoting Noncanonical WNT Signaling.

Authors:  Kenji Kato; Pallavi Bhattaram; Alfredo Penzo-Méndez; Abhilash Gadi; Véronique Lefebvre
Journal:  J Bone Miner Res       Date:  2015-05-21       Impact factor: 6.741

7.  The impairment of MAGMAS function in human is responsible for a severe skeletal dysplasia.

Authors:  Cybel Mehawej; Agnès Delahodde; Laurence Legeai-Mallet; Valérie Delague; Nabil Kaci; Jean-Pierre Desvignes; Zoha Kibar; José-Mario Capo-Chichi; Eliane Chouery; Arnold Munnich; Valérie Cormier-Daire; André Mégarbané
Journal:  PLoS Genet       Date:  2014-05-01       Impact factor: 5.917

8.  The first case of Horn Kolb Syndrome in Turkey, diagnosed prenatally at the 23(rd) week of a pregnancy: A very rare and unusual case far from the original geography.

Authors:  Ismail Temur; Kahraman Ulker; Islim Volkan; Mehmet Karaca; Mustafa Ersoz; Abdulaziz Gul; Esat Adiguzel
Journal:  Am J Case Rep       Date:  2012-06-13

Review 9.  Guidelines for genetic skeletal dysplasias for pediatricians.

Authors:  Sung Yoon Cho; Dong-Kyu Jin
Journal:  Ann Pediatr Endocrinol Metab       Date:  2015-12-31
  9 in total

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