Literature DB >> 7981854

Radial ray defects, renal ectopia, duodenal atresia and hydrocephalus: the extended spectrum for Fanconi anaemia.

D G Evans1, H C Rees, A Spreadborough, D J Campbell, G S Gau, E Pickering, S Hamilton, J Clayton-Smith.   

Abstract

We present two families with a striking concordance of multiple anomalies. These include duodenal and other bowel atresia, radial ray defects especially absent or vestigial thumb, renal ectopia and hydrocephalus. The presence of diagnostically raised sensitivity to mitomycin C in the first family has confirmed Fanconi anaemia. This has further increased the spectrum of abnormalities in Fanconi anaemia and highlights the importance of mitomycin C analysis if elements of this spectrum are encountered.

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Year:  1994        PMID: 7981854

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN: 0962-8827            Impact factor:   0.816


  1 in total

1.  The Fanconi anemia group E gene, FANCE, maps to chromosome 6p.

Authors:  Q Waisfisz; K Saar; N V Morgan; C Altay; P A Leegwater; J P de Winter; K Komatsu; G R Evans; R D Wegner; A Reis; H Joenje; F Arwert; C G Mathew; J C Pronk; M Digweed
Journal:  Am J Hum Genet       Date:  1999-05       Impact factor: 11.025

  1 in total

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