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Results 1 - 8 of 8 for Esophageal atresia
  1. Esophageal atresia/tracheoesophageal fistula 
    Esophageal atresia/tracheoesophageal fistula (EA/TEF) is a condition resulting from abnormal development before birth of the tube ... occur properly, EA/TEF is the result.In esophageal atresia (EA), the upper esophagus does not connect (atresia) ...
    https://medlineplus.gov/...phageal-atresia-tracheoesophageal-fistula - Genetics
  2. Opitz G/BBB syndrome 
    ... of the disorder in their family. Hypertelorism with esophageal abnormalities and hypospadias Hypertelorism-hypospadias sydrome Hypospadias-dysphagia syndrome ...
    https://medlineplus.gov/genetics/condition/opitz-g-bbb-syndrome - Genetics
  3. Mandibulofacial dysostosis with microcephaly 
    ... this disorder also have blockage of the esophagus (esophageal atresia). In esophageal atresia, the upper esophagus does not connect to the lower esophagus and stomach. Most babies born with esophageal atresia (EA) also have a tracheoesophageal fistula (TEF), in ...
    https://medlineplus.gov/...dibulofacial-dysostosis-with-microcephaly - Genetics
  4. SOX2 anophthalmia syndrome 
    ... this condition are born with a blocked esophagus (esophageal atresia), which is often accompanied by an abnormal connection ... Syndromic microphthalmia 3 Genetic Testing Registry: ... Anophthalmia/microphthalmia-esophageal atresia syndrome National Organization ...
    https://medlineplus.gov/.../condition/sox2-anophthalmia-syndrome - Genetics
  5. Feingold syndrome 
    ... most cases, the blockage occurs in the esophagus (esophageal atresia) or in part of the small intestine (duodenal ...
    https://medlineplus.gov/genetics/condition/feingold-syndrome - Genetics
  6. Cartilage-hair hypoplasia 
    ... anus (anal stenosis) or blockage of the esophagus (esophageal atresia) may also occur. Cartilage-hair hypoplasia occurs most ...
    https://medlineplus.gov/genetics/condition/cartilage-hair-hypoplasia - Genetics
  7. VACTERL association 
    ... for vertebral defects, anal atresia, cardiac defects, tracheo-esophageal fistula, renal anomalies, and limb abnormalities. People diagnosed with VACTERL association typically have at ...
    https://medlineplus.gov/genetics/condition/vacterl-association - Genetics
  8. Systemic scleroderma 
    ... common features of the condition: calcinosis, Raynaud phenomenon, esophageal motility dysfunction, sclerodactyly, and telangiectasia. In another type ...
    https://medlineplus.gov/genetics/condition/systemic-scleroderma - Genetics