Literature DB >> 6390321

Hydrolethalus syndrome in consecutive African siblings.

O O Adetoro, F Komolafe, A Anjorin.   

Abstract

Hydrolethalus syndrome may comprise mainly hydrocephalus, polydactyly, micrognathia, congenital cardiac and respiratory anomalies and uniform lethality. It was recently described in Finland, with a suggestion that it might be one of the "Finnish" diseases [4]. We report two cases of this syndrome in consecutive siblings of a Nigerian couple. In addition, we describe associated healing fractures of the long bones, a feature not mentioned in the original report, apparently because those cases were not subjected to post-partum radiography.

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Year:  1984        PMID: 6390321     DOI: 10.1007/BF02343433

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


  2 in total

1.  Causes of congenital malformations in human beings.

Authors:  F C FRASER
Journal:  J Chronic Dis       Date:  1959-08

2.  The hydrolethalus syndrome: delineation of a "new", lethal malformation syndrome based on 28 patients.

Authors:  R Salonen; R Herva; R Norio
Journal:  Clin Genet       Date:  1981-05       Impact factor: 4.438

  2 in total
  1 in total

1.  Hydrolethalus syndrome.

Authors:  R Salonen; R Herva
Journal:  J Med Genet       Date:  1990-12       Impact factor: 6.318

  1 in total

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