Literature DB >> 6807992

Two clinical variants of spondylo-epiphysial dysplasia congenita.

R Wynne-Davies, C Hall.   

Abstract

Seventeen patients with congenital spondylo-epiphysial dysplasia from six centres in Britain have been investigated and two variants delineated. There is wide clinical and radiological variability in each group with overlap between them, but 12 of the patients had very short stature and grossly disorganised hips with severe coxa vara, and the five remaining patients were less seriously affected with height only a little below the third percentile and only mild coxa vara. Both groups can be diagnosed at birth but the two cannot be differentiated on clinical and radiological grounds until after the age of three to four years when the developing severe coxa vara and difference in stature become apparent. All cases were sporadic with the exception of a concordant twin-pair.

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Year:  1982        PMID: 6807992     DOI: 10.1302/0301-620X.64B4.6807992

Source DB:  PubMed          Journal:  J Bone Joint Surg Br        ISSN: 0301-620X


  4 in total

1.  Lethal skeletal dysplasia owing to double heterozygosity for achondroplasia and spondyloepiphyseal dysplasia congenita.

Authors:  I D Young; N R Ruggins; J M Somers; J M Zuccollo; N Rutter
Journal:  J Med Genet       Date:  1992-11       Impact factor: 6.318

2.  Identification of an Autosomal Dominant Mutation in the COL2A1 Gene Leading to Spondyloepiphyseal Dysplasia Congenita in a Greek Family.

Authors:  Εirini Dikaiakou; Εlpis A Vlachopapadopoulou; Emanouil Manolakos; Panagiotis Samelis; Rodanthi Margariti; Christos Zampakides; Stefanos Michalacos
Journal:  Mol Syndromol       Date:  2018-08-31

3.  The fate of the hip in spondylo-epi-metaphyseal dysplasia: clinical and radiological evaluation of adults with SEMD Handigodu type.

Authors:  N D Siddesh; Hitesh Shah; Benjamin Joseph
Journal:  Skeletal Radiol       Date:  2011-11-25       Impact factor: 2.199

4.  Epiphyseal dysplasia of the femoral head, mild vertebral abnormality, myopia, and sensorineural deafness: report of a pedigree with autosomal dominant inheritance.

Authors:  K D MacDermot; S C Roth; C Hall; R M Winter
Journal:  J Med Genet       Date:  1987-10       Impact factor: 6.318

  4 in total

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