Genetic factors in isolated and syndromic esophageal atresia

J Pediatr Gastroenterol Nutr. 2011 May:52 Suppl 1:S6-8. doi: 10.1097/MPG.0b013e318213316a.
No abstract available

MeSH terms

  • Anal Canal / abnormalities
  • Anemia, Megaloblastic / complications
  • CHARGE Syndrome / complications
  • Chromosome Aberrations
  • Diabetes Mellitus
  • Duodenal Obstruction / complications
  • Environmental Exposure / adverse effects
  • Esophageal Atresia / classification
  • Esophageal Atresia / complications
  • Esophageal Atresia / etiology*
  • Esophageal Atresia / genetics*
  • Esophagus / abnormalities
  • Eyelids / abnormalities
  • Fanconi Anemia / complications
  • Female
  • Hearing Loss, Sensorineural / complications
  • Heart Defects, Congenital / complications
  • Humans
  • Intellectual Disability
  • Ketoglutarate Dehydrogenase Complex / deficiency
  • Kidney / abnormalities
  • Limb Deformities, Congenital / complications
  • Maternal Exposure / adverse effects
  • Microcephaly / complications
  • Mutation
  • Pregnancy
  • Spine / abnormalities
  • Thiamine Deficiency / congenital
  • Trachea / abnormalities
  • Tracheoesophageal Fistula / genetics

Substances

  • Ketoglutarate Dehydrogenase Complex

Supplementary concepts

  • Oculodigitoesophagoduodenal syndrome
  • Thiamine responsive megaloblastic anemia syndrome
  • VACTERL association