Trisomy 18 syndrome: Case report
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Case Reports
P: 44-46
March 2012

Trisomy 18 syndrome: Case report

Med J Bakirkoy 2012;8(1):44-46
1. Erzurum Nenehatun Kadın Doğum Hastanesi, Genetik Ünitesi, Erzurum
2. Erzurum Nenehatun Kadın Doğum Hastanesi, Yenidoğan Ünitesi, Erzurum
No information available.
No information available
Received Date: 20.07.2010
Accepted Date: 24.02.2011
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ABSTRACT

In trisomy 18 (Edward’s) syndrome, which is one of the most common chromosomal disorders, most of the cases are lost during their first year of life because of severe cardiac pathologies. A female premature newborn with a weight of 1100 g was referred to our clinic by dyspnea. At the physical examination, low ears, high arched palate, migrognatia, short and webbed neck, microcephaly, flexed hand fingers and pes equinovarus of foot were present. At the echocardiography examination, patent ductus arteriosus has been detected. Herein we presented this case with Edward’s syndrome with clear clinical evidence in newborn period.

Keywords: Trisomy 18 syndrome, newborn, pes equinovarus

References

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