Literature DB >> 10076879

VACTERL as primary, polytopic developmental field defects.

M L Martínez-Frías1, J L Frías.   

Abstract

Previously we proposed that the VACTERL association represents a dysmorphogenetic response of the primary developmental field, i.e., polytopic developmental field defects (DFD). As such, it should conform to the essential attributes of a DFD, namely, heterogeneity, homology, and phylogeneity. To study its heterogeneity, we analyzed the data of the Spanish Collaborative Study of Congenital Malformations (ECEMC). Our results confirm the observations indicating that the different patterns of defects that constitute this entity are not only clinically variable but also causally heterogeneous. This causal heterogeneity, which is of crucial importance in defining developmental fields, gives additional credence to the hypothesis that VACTERL constitutes a primary polytopic DFD.

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Year:  1999        PMID: 10076879     DOI: 10.1002/(sici)1096-8628(19990305)83:1<13::aid-ajmg4>3.3.co;2-o

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  12 in total

1.  Molecular genetic analysis of a de novo balanced translocation t(6;17)(p21.31;q11.2) associated with hypospadias and anorectal malformation.

Authors:  Mahmoud Reza Mansouri; Birgit Carlsson; Edward Davey; Agneta Nordenskjöld; Tomas Wester; Göran Annerén; Göran Läckgren; Niklas Dahl
Journal:  Hum Genet       Date:  2006-01-03       Impact factor: 4.132

2.  Considering the Embryopathogenesis of VACTERL Association.

Authors:  R E Stevenson; A G W Hunter
Journal:  Mol Syndromol       Date:  2013-02

Review 3.  Oesophageal atresia, tracheo-oesophageal fistula, and the VACTERL association: review of genetics and epidemiology.

Authors:  C Shaw-Smith
Journal:  J Med Genet       Date:  2005-11-18       Impact factor: 6.318

Review 4.  Congenital and idiopathic scoliosis: clinical and genetic aspects.

Authors:  Philip F Giampietro; Robert D Blank; Cathleen L Raggio; Sajid Merchant; F Stig Jacobsen; Thomas Faciszewski; Sanjay K Shukla; Anne R Greenlee; Cory Reynolds; David B Schowalter
Journal:  Clin Med Res       Date:  2003-04

Review 5.  Postmarketing analysis of medicines: methodology and value of the spanish case-control study and surveillance system in preventing birth defects.

Authors:  María Luisa Martínez-Frías
Journal:  Drug Saf       Date:  2007       Impact factor: 5.606

6.  A neonate with anorectal malformation with rare limb defects report of a case.

Authors:  Simmi K Ratan; Kamal Nain Rattan; John Ratan; Punita Kumari Sodhi; Vipin Bhatia
Journal:  Pediatr Surg Int       Date:  2005-10-21       Impact factor: 1.827

7.  Loss of the Sall3 gene leads to palate deficiency, abnormalities in cranial nerves, and perinatal lethality.

Authors:  M Parrish; T Ott; C Lance-Jones; G Schuetz; A Schwaeger-Nickolenko; A P Monaghan
Journal:  Mol Cell Biol       Date:  2004-08       Impact factor: 4.272

8.  Associated anomalies with anorectal malformation (ARM).

Authors:  Amit Mittal; Raj Kumar Airon; Sarita Magu; Kamal Nain Rattan; Simmi K Ratan
Journal:  Indian J Pediatr       Date:  2004-06       Impact factor: 1.967

9.  Is Duane retraction syndrome part of the VACTERL association?

Authors:  Serpil Akar; Birsen Gokyigit; Isilay Kavadarli; Ahmet Demirok
Journal:  Clin Ophthalmol       Date:  2013-03-20

10.  Esophageal atresia in newborns: a wide spectrum from the isolated forms to a full VACTERL phenotype?

Authors:  Simona La Placa; Mario Giuffrè; Antonella Gangemi; Stefania Di Noto; Federico Matina; Federica Nociforo; Vincenzo Antona; Maria Rita Di Pace; Maria Piccione; Giovanni Corsello
Journal:  Ital J Pediatr       Date:  2013-07-10       Impact factor: 2.638

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