Literature DB >> 6489381

Ruvalcaba syndrome: a case report.

E Bianchi, C Livieri, M Arico, E Cattaneo, A F Podesta, G Beluffi.   

Abstract

An 11-year-old child with mental retardation and short stature was examined and found to be affected with some skeletal malformations. The clinical and radiological pattern of limb alterations was particularly suggestive of the features of Ruvalcaba syndrome. A complete examination confirmed the diagnosis and showed ocular involvement. To the best of our knowledge this is first published confirmation of Ruvalcaba syndrome.

Entities:  

Mesh:

Year:  1984        PMID: 6489381     DOI: 10.1007/bf00540259

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  2 in total

1.  A 'new' syndrome of mental retardation with characteristic facies and brachyphalangy.

Authors:  A G Hunter; P J McAlpine; N L Rudd; F C Fraser
Journal:  J Med Genet       Date:  1977-12       Impact factor: 6.318

2.  A new familial syndrome with osseous dysplasia and mental dificiency.

Authors:  R H Ruvalcaba; A Reichert; D W Smith
Journal:  J Pediatr       Date:  1971-09       Impact factor: 4.406

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.