Literature DB >> 641954

Familial radioulnar synostosis.

R A Spritz.   

Abstract

A family with proximal radioulnar synostosis segregating in three generations is described. Familial radioulnar synostosis is a rare anomaly; however, the sporadic form is a frequent feature in cases of sex chromosome abnormalities and other syndromes. This disorder has been reported in several ethnic groups, but this is apparently the first example from the black population.

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Year:  1978        PMID: 641954      PMCID: PMC1013669          DOI: 10.1136/jmg.15.2.160

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  5 in total

1.  Swivel for proximal radio-ulnar synostosis.

Authors:  H KELIKIAN; A DOUMANIAN
Journal:  J Bone Joint Surg Am       Date:  1957-07       Impact factor: 5.284

2.  Radioulnar synostosis and craniosynostosis in one family.

Authors:  M Berant; N Berant
Journal:  J Pediatr       Date:  1973-07       Impact factor: 4.406

3.  Congenital radio-ulnar synostosis. Report of 37 cases.

Authors:  O H Hansen; N O Andersen
Journal:  Acta Orthop Scand       Date:  1970

4.  Radioulnar synostosis, behavioral disturbance, and XYY chromosomes.

Authors:  W W Cleveland; D Arias; G F Smith
Journal:  J Pediatr       Date:  1969-01       Impact factor: 4.406

5.  Radioulnar synostosis. A common occurrence in sex chromosomal abnormalities.

Authors:  J Jancu
Journal:  Am J Dis Child       Date:  1971-07
  5 in total
  3 in total

1.  The developmental spectrum of proximal radioulnar synostosis.

Authors:  Alison M Elliott; Lisa Kibria; Martin H Reed
Journal:  Skeletal Radiol       Date:  2010-01       Impact factor: 2.199

2.  Oligodactyly and multiple synostoses of the extremities: two cases in sibs. A variant of Cenani-Lenz syndactyly.

Authors:  P Dodinval
Journal:  Hum Genet       Date:  1979-04-27       Impact factor: 4.132

3.  A genotype and phenotype analysis of SMAD6 mutant patients with radioulnar synostosis.

Authors:  Fang Shen; Yongjia Yang; Pengcheng Li; Yu Zheng; Zhenqing Luo; Yuyan Fu; Guanghui Zhu; Haibo Mei; Shanlin Chen; Yimin Zhu
Journal:  Mol Genet Genomic Med       Date:  2021-12-24       Impact factor: 2.183

  3 in total

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