Literature DB >> 18706355

[Sirenomelia as a part of VACTERL association: a study of three cases].

Philippe Charlier1, Anne-Sylvie Valat, Odile Boute, Stéphanie Petit, Caroline Chafiotte, Isabelle Huynh-Charlier, Bernard Gosselin, Louise Devisme.   

Abstract

Sirenomelia, characterized by a fusion of lower limb buds, is rare. Moreover, the coexistence of this malformation with a VACTERL sequence is exceptional. We report, here, three new observations associating these two diseases on fetuses from 14 to 26 weeks gestation. With these three new cases associating sirenomelia and VACTERL, observed in our unit and examined in light of data from the medical literature, we discuss the embryologic origin of such malformations and the nosologic frontiers between these two diseases.

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Year:  2008        PMID: 18706355     DOI: 10.1016/j.annpat.2008.06.001

Source DB:  PubMed          Journal:  Ann Pathol        ISSN: 0242-6498            Impact factor:   0.407


  1 in total

1.  Sirenomelia and severe caudal regression syndrome.

Authors:  Mohammed Z Seidahmed; Omer B Abdelbasit; Khalid A Alhussein; Abeer M Miqdad; Mohammed I Khalil; Mustafa A Salih
Journal:  Saudi Med J       Date:  2014-12       Impact factor: 1.484

  1 in total

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