Literature DB >> 1671807

Mild spondyloepiphyseal dysplasia (Namaqualand type): genetic linkage to the type II collagen gene COL2A1.

C Sher1, R Ramesar, R Martell, I Learmonth, P Tsipouras, P Beighton.   

Abstract

Namaqualand spondyloepiphyseal dysplasia (NSED) is a mild autosomal dominant form of spondyloepiphyseal dysplasia in which changes are maximal in the femoral capital epiphyses and the vertebral bodies. The condition is present in a large multigeneration South African family, and it is clinically important by virtue of severe progressive degenerative osteoarthropathy of the hip joint, which frequently necessitates prosthetic joint replacement in adulthood. Linkage studies using molecular markers have shown that the loci for the NSED and type II collagen genes are linked (LOD score 7.98 at a recombination fraction of .00).

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Year:  1991        PMID: 1671807      PMCID: PMC1682978     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  21 in total

1.  Genetic linkage of a polymorphism in the type II procollagen gene (COL2A1) to primary osteoarthritis associated with mild chondrodysplasia.

Authors:  R G Knowlton; P L Katzenstein; R W Moskowitz; E J Weaver; C J Malemud; M N Pathria; S A Jimenez; D J Prockop
Journal:  N Engl J Med       Date:  1990-02-22       Impact factor: 91.245

2.  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

3.  Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.

Authors:  L M Kunkel; K D Smith; S H Boyer; D S Borgaonkar; S S Wachtel; O J Miller; W R Breg; H W Jones; J M Rary
Journal:  Proc Natl Acad Sci U S A       Date:  1977-03       Impact factor: 11.205

4.  Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies.

Authors:  J Ott
Journal:  Am J Hum Genet       Date:  1974-09       Impact factor: 11.025

5.  Namaqualand hip dysplasia: an autosomal dominant entity.

Authors:  P Beighton; G Christy; I D Learmonth
Journal:  Am J Med Genet       Date:  1984-09

6.  "A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum.

Authors:  A P Feinberg; B Vogelstein
Journal:  Anal Biochem       Date:  1984-02       Impact factor: 3.365

7.  Cartilage collagen analysis in the chondrodystrophies.

Authors:  W A Horton; J W Chou; M A Machado
Journal:  Coll Relat Res       Date:  1985-09

8.  Single base mutation in the type II procollagen gene (COL2A1) as a cause of primary osteoarthritis associated with a mild chondrodysplasia.

Authors:  L Ala-Kokko; C T Baldwin; R W Moskowitz; D J Prockop
Journal:  Proc Natl Acad Sci U S A       Date:  1990-09       Impact factor: 11.205

9.  Spondyloepiphyseal dysplasia congenita: genetic linkage to type II collagen (COL2AI).

Authors:  I J Anderson; R B Goldberg; R W Marion; W B Upholt; P Tsipouras
Journal:  Am J Hum Genet       Date:  1990-05       Impact factor: 11.025

10.  Nonexpression of cartilage type II collagen in a case of Langer-Saldino achondrogenesis.

Authors:  D R Eyre; M P Upton; F D Shapiro; R H Wilkinson; G F Vawter
Journal:  Am J Hum Genet       Date:  1986-07       Impact factor: 11.025

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  3 in total

Review 1.  The type II collagenopathies: a spectrum of chondrodysplasias.

Authors:  J Spranger; A Winterpacht; B Zabel
Journal:  Eur J Pediatr       Date:  1994-02       Impact factor: 3.183

2.  A missense mutation in the mouse Col2a1 gene causes spondyloepiphyseal dysplasia congenita, hearing loss, and retinoschisis.

Authors:  Leah Rae Donahue; Bo Chang; Subburaman Mohan; Nao Miyakoshi; Jon E Wergedal; David J Baylink; Norman L Hawes; Clifford J Rosen; Patricia Ward-Bailey; Qing Y Zheng; Roderick T Bronson; Kenneth R Johnson; Muriel T Davisson
Journal:  J Bone Miner Res       Date:  2003-09       Impact factor: 6.741

3.  Spondyloepiphyseal dysplasia and precocious osteoarthritis in a family with an Arg75-->Cys mutation in the procollagen type II gene (COL2A1).

Authors:  C J Williams; E L Considine; R G Knowlton; A Reginato; G Neumann; D Harrison; P Buxton; S Jimenez; D J Prockop
Journal:  Hum Genet       Date:  1993-11       Impact factor: 4.132

  3 in total

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