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Case Report

VACTERL Association: A New Case with Biotinidase Deficiency and Annular Pancreas

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Pages 123-125 | Received 01 Jun 2011, Accepted 11 Sep 2011, Published online: 20 Oct 2011

REFERENCES

  • de Jong EM, Felix JF, Deurloo JA, . Non-VACTERL-type anomalies are frequent in patients with esophageal atresia/tracheo-esophageal fistula and full or partial VACTERL association. Birth Defects Res A Clin Mol Teratol. 2008;82:92–97.
  • Jones KL. Miscellaneous syndromes, VATER association. In: Hummel T, ed. Smiths Recognizable Patterns of Human Malformation. 6th ed. Philadelphia, PA: Elsevier; 2006:578–579.
  • Reardon W, Zhou XP, Eng C. A novel germline mutation of the PTEN gene in a patient with macrocephaly, ventricular dilatation and features of VATER association. J Med Genet. 2001;38:820–823.
  • van den Brink GR. Hedgehog signaling in development and homeostasis of the gastrointestinal tract. Physiol Rev. 2007;87:1343–1375.

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