Unusual Clinical History of a Male Infant with Edwards Syndrome

Abstract

Edwards syndrome (trisomy of chromosome 18) is generally characterized by the disorders of central nervous system, as well as the musculoskeletal and genitourinary systems. In majority of the cases with trisomy 18 the following malformations can be found: ventricular septal defect, horseshoe kidneys, oesophageal atresia, omphalocele, facial clefts, diaphragmatic hernias and genital hypoplasia. We report a male patient with Edwards syndrome. The boy had a partial agenesis of corpus callosum, oesophageal atresia with tracheo-oesophageal fistula, renal agenesis, ventricular septal defect, Dandy-Walker cyst and low-set malformed ears. The first three features are unique based on previous literature reports on trisomy 18. This report allows a further delineation of the trisomy 18 syndrome.

DOI: 10.1007/s12253-008-9023-2

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Cite this paper

@article{Surnyi2008UnusualCH, title={Unusual Clinical History of a Male Infant with Edwards Syndrome}, author={Andrea Sur{\'a}nyi and Tam{\'a}s Bit{\'o} and Gy{\"{o}rgy Vajda and L{\'a}szl{\'o} Kaiser and G{\'a}bor G{\'a}sp{\'a}r and M{\'a}rta Katona and Janos Szabo and Attila P{\'a}l}, journal={Pathology & Oncology Research}, year={2008}, volume={15}, pages={147-152} }