Vertebral anomalies in a new family with ODED syndrome
- 1 June 2000
- journal article
- case report
- Published by Wiley in Clinical Genetics
- Vol. 57 (6), 444-448
- https://doi.org/10.1034/j.1399-0004.2000.570608.x
Abstract
We report a new family with oculodigitoesophagoduodenal syndrome (ODED syndrome), which associates microcephaly, abnormalities of the hands and feet, shortened palpebral fissures, tracheoesophageal fistula and duodenal atresia. In addition, previously unreported vertebral anomalies are described. This report further delineates the clinical and radiographic spectrum of this syndrome, providing useful information for diagnosis and family counseling.Keywords
This publication has 9 references indexed in Scilit:
- Maternal Thyroid Deficiency during Pregnancy and Subsequent Neuropsychological Development of the ChildNew England Journal of Medicine, 1999
- Feingold syndrome: Report of a new family and reviewAmerican Journal of Medical Genetics, 1997
- MODED: Microcephaly-oculo-digito-esophageal-duodenal syndromeAmerican Journal of Medical Genetics, 1997
- Autosomal dominant microcephaly with normal intelligence, short palpebral fissures, and digital anomaliesAmerican Journal of Medical Genetics, 1997
- The spectrum of congenital anomalies of the VATER association: An international studyAmerican Journal of Medical Genetics, 1997
- Syndrome of microcephaly, facial and hand abnormalities, tracheoesophageal fistula, duodenal atresia, and developmental delayAmerican Journal of Medical Genetics, 1997
- Digital anomalies, microcephaly, and normal intelligence: New syndrome or Feingold syndrome?American Journal of Medical Genetics, 1997
- Autosomal dominant inheritance of abnormalities of the hands and feet with short palpebral fissures, variable microcephaly with learning disability, and oesophageal/duodenal atresia.Journal of Medical Genetics, 1991
- An Unusual MicrocephalyHospital Practice, 1978