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Disease: Esophageal duodenal atresia abnormalities of hands

  • A Feingold syndrome case with previously undescribed features and a new mutation
  • Autosomal dominant inheritance of abnormalities of the hands and feet with short palpebral fissures, variable microcephaly with learning disability, and oesophageal/duodenal atresia
  • Evaluation of a new slim radial echoendoscope: A better option for an aging population
  • Familial syndromic duodenal atresia: Feingold syndrome
  • Feingold syndrome
  • Feingold syndrome: report of a new family and review
  • Gastrointestinal function in chronic renal failure
  • Generalized overconstriction of long bones and unilateral Kirner's deformity in a deLange dwarf
  • Growth deficiency in oculodigitoesophagoduodenal (Feingold) syndrome--case report and review of the literature
  • How many entities exist for the spectrum of disorders associated with brachydactyly, syndactyly, short stature, microcephaly, and intellectual disability?
  • Hydramnios and fetal malformations. Use of estimating the level of alpha-fetoprotein and of bilirubin in the amniotic fluid during the last trimester of pregnancy (author's transl)
  • Imperforate anus in Feingold syndrome
  • MODED: microcephaly-oculo-digito-esophageal-duodenal syndrome
  • The shape of the duodenal loop. Radiological, physiological and clinical aspects in patients with X-ray negative dyspepsia
  • Vertebral defects in a patient with Feingold syndrome
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