Literature DB >> 1488984

Tracheoesophageal fistula, gastrointestinal abnormalities, hypospadias, and prenatal growth deficiency.

M L Martínez-Frías1, J L Frías, E Galán, R Domingo, L Paisán, M Blanco.   

Abstract

We studied 2 sibs, born to consanguineous parents, who presented with an MCA pattern which includes low birthweight, tracheoesophageal fistula, duodenal atresia, extrahepatic biliary atresia, hypoplastic pancreas, and hypospadias. This constellation of congenital anomalies appears to be a previously unreported autosomal recessive syndrome. A computerized search of the data files of the Spanish Collaborative Study of Congenital Malformations (ECEMC) identified 3 other unrelated infants with intestinal atresias, hypospadias, and low birth weight. These cases may represent a milder expression of the same syndrome.

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Mesh:

Year:  1992        PMID: 1488984     DOI: 10.1002/ajmg.1320440316

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


  10 in total

1.  Fetal liver iron overload: the role of MR imaging.

Authors:  Marie Cassart; Freddy Efraim Avni; Laurent Guibaud; Marc Molho; Nicky D'Haene; Alain Paupe
Journal:  Eur Radiol       Date:  2010-09-04       Impact factor: 5.315

Review 2.  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

3.  Neonatal diabetes, with hypoplastic pancreas, intestinal atresia and gall bladder hypoplasia: search for the aetiology of a new autosomal recessive syndrome.

Authors:  J Mitchell; Z Punthakee; B Lo; C Bernard; K Chong; C Newman; L Cartier; V Desilets; E Cutz; I L Hansen; P Riley; C Polychronakos
Journal:  Diabetologia       Date:  2004-12-08       Impact factor: 10.122

4.  Achondroplasia and Biliary Atresia: A Rare Association and Review of Literature.

Authors:  Ranjit I Kylat
Journal:  J Pediatr Genet       Date:  2017-01-02

5.  Clinical and genetic complexity of Mitchell-Riley/Martinez-Frias syndrome.

Authors:  L Cruz; R E Schnur; E M Post; H Bodagala; R Ahmed; C Smith; L B Lulis; G E Stahl; A Kushnir
Journal:  J Perinatol       Date:  2014-12       Impact factor: 2.521

Review 6.  Review of genetic factors in intestinal malrotation.

Authors:  Vicki Martin; Charles Shaw-Smith
Journal:  Pediatr Surg Int       Date:  2010-06-13       Impact factor: 1.827

7.  A fate map of the murine pancreas buds reveals a multipotent ventral foregut organ progenitor.

Authors:  Jesse R Angelo; Mara-Isel Guerrero-Zayas; Kimberly D Tremblay
Journal:  PLoS One       Date:  2012-07-17       Impact factor: 3.240

Review 8.  Direct Lineage Reprogramming: Harnessing Cell Plasticity between Liver and Pancreas.

Authors:  Silvia Ruzittu; David Willnow; Francesca M Spagnoli
Journal:  Cold Spring Harb Perspect Biol       Date:  2020-07-01       Impact factor: 9.708

9.  Cecum perforation in intestinal malrotation setting in a patient with chromosome 12p deletion syndrome: A case report.

Authors:  João T Oliveira; Paula Marques; J M Preza Fernandes; Tânia Teixeira; Marisa D Santos; Ana Povo; Eurico Castro Alves
Journal:  Int J Surg Case Rep       Date:  2019-12-17

10.  A Newly-Discovered Mutation in the RFX6 Gene of the Rare Mitchell-Riley Syndrome.

Authors:  Nusrat Khan; Waleed Dandan; Noura Al Hassani; Suha Hadi
Journal:  J Clin Res Pediatr Endocrinol       Date:  2015-01-18
  10 in total

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