Trisomy 18 Syndrome: A Case Report
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Case Report
P: 109-111
April 2015

Trisomy 18 Syndrome: A Case Report

Eur Arc Med Res 2015;31(2):109-111
1. Bolu İzzet Baysal Devlet Hastanesi, Çocuk Sağlığı ve Hastalıkları
2. Bolu Abant İzzet Baysal Üniversitesi, Çocuk Sağlığı ve Hastalıkları
No information available.
No information available
Received Date: 19.04.2014
Accepted Date: 08.09.2014
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ABSTRACT

Trisomy 18 (Edwards syndrome), is a syndrome characterized by multiple congenital anomalies, occuring together with excess 18. chromosome. Intrauterine growth retardation, micrognathia, microcephaly, low-set ears, cardiac abnormalities, urinary tract abnormalities, gastrointestinal tract anomalies and limb anomalies are the findings which are commonly encountered in infants with Edwards Syndrome. Here we aimed to present a case of 2 months old infant with multiple congenital anomalies and diagnosed as Edwards Syndrome.

Keywords:
trisomy 18, congenital heart disease, limb abnormalities