Literature DB >> 7936797

Japanese type of spondylo-metaphyseal dysplasia.

T Hasegawa1, K Kozlowski, G Nishimura, H Hara, Y Hasegawa, T Aso, S Koto, T Nagai, Y Tsuchiya.   

Abstract

Five members of a Japanese family with a new form of spondylo-metaphyseal dysplasia (SMD) are reported. Another member was also probably affected. The disease was characterised by severe coxa vara, moderately severe metaphyseal changes of the long bones of the lower limbs, mild changes in the long bones of the upper limbs and grossly normal short tubular bones. Platyspondyly, present in the boys, was less marked in their father, whereas two affected aunts had normally shaped vertebral bodies.

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Year:  1994        PMID: 7936797     DOI: 10.1007/bf02012189

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


  9 in total

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Journal:  Radiol Med       Date:  1993 Jan-Feb       Impact factor: 3.469

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  9 in total
  3 in total

Review 1.  Genetic analysis of skeletal dysplasia: recent advances and perspectives in the post-genome-sequence era.

Authors:  Shiro Ikegawa
Journal:  J Hum Genet       Date:  2006-05-03       Impact factor: 3.172

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Journal:  Am J Hum Genet       Date:  1998-12       Impact factor: 11.025

3.  A novel sequence variant in COL10A1 causing spondylometaphyseal dysplasia accompanied with coxa valga: A case report.

Authors:  Xianzuo Zhang; Haiyi Liang; Weilu Liu; Xu Li; Wenzhi Zhang; Xifu Shang
Journal:  Medicine (Baltimore)       Date:  2019-07       Impact factor: 1.817

  3 in total

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