Literature DB >> 23365163

Short-term surviving sirenomelia neonate followed by a complex mesodermal malformation in a sibling.

Giuliano Rigon1, Cristina Vallone, Evelina Silvestri, Fabrizio Signore.   

Abstract

Mesh：

Year:  2013        PMID： 23365163      PMCID： PMC3603659          DOI： 10.1136/bcr-2012-007941

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN： 1757-790X


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  3 in total

1.  A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis.

Authors:  A J Ross; V Ruiz-Perez; Y Wang; D M Hagan; S Scherer; S A Lynch; S Lindsay; E Custard; E Belloni; D I Wilson; R Wadey; F Goodman; K H Orstavik; T Monclair; S Robson; W Reardon; J Burn; P Scambler; T Strachan
Journal:  Nat Genet       Date:  1998-12       Impact factor: 38.330

Review 2.  Sirenomelia, the Mermaid syndrome: case report and a brief review of literature.

Authors:  Rozina Sikandar; Shama Munim
Journal:  J Pak Med Assoc       Date:  2009-10       Impact factor: 0.781

3.  Clusters of sirenomelia in South America.

Authors:  Iêda M Orioli; Pierpaolo Mastroiacovo; Jorge S López-Camelo; Wilmar Saldarriaga; Carolina Isaza; Horacio Aiello; Ignacio Zarante; Eduardo E Castilla
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2009-02
  3 in total
  1 in total

1.  What is your diagnosis?

Authors:  İlknur Adanır; Ayşe Filiz Gökmen Karasu; Banu Dane
Journal:  J Turk Ger Gynecol Assoc       Date:  2017-12-15
  1 in total

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