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Volume: 55 Issue: 1 Year: 2024

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Bilateral Renal Agenesis and Aortic Stenosis in an Antenatally Diagnosed Turner Syndrome [Zeynep Kamil Med J]
Zeynep Kamil Med J. 2016; 47(4): 128-131 | DOI: 10.16948/zktipb.237205

Bilateral Renal Agenesis and Aortic Stenosis in an Antenatally Diagnosed Turner Syndrome

Handan Hakyemez Toptan1, Nilgün Karadağ1, Abdülhamit Tüten1, Tülin Gökmen Yıldırım1, Gülsen Akay2, Mehmet Burak Kutlu3, Güner Karatekin1
1Zeynep Kamil Obstetrics and Pediatrics Training. Res. Hospital, Neonatal Intensive Care Unit, Istanbul
2Zeynep Kamil Obstetrics and Pediatrics Training and Research Hospital, Pediatric Genetics Department, Istanbul
3Zeynep Kamil Obstetrics and Pediatrics Training and Research Hospital, Department of Medical Genetics, Istanbul

Turner syndrome is a genetic disorder caused by loss or structural disorders of X chromosome. A significant number of cases result with abortion. Clinical symptoms are not always apparent in the newborn period. Therefore it could be diagnosed in later years of life. Turner syndrome should be considered in patients with lymphedema on hands and feets, low hairline, short and webbed neck. Cardiovascular, genitourinary, endocrine system disorders could be accompanied. Here we present an antenatally diagnosed Turner syndrome with bilateral renal agenesis, pulmonary hypoplasia and aortic stenosis.

Keywords: Aortic stenosis, Renal agenesis; Turner syndrome

Handan Hakyemez Toptan, Nilgün Karadağ, Abdülhamit Tüten, Tülin Gökmen Yıldırım, Gülsen Akay, Mehmet Burak Kutlu, Güner Karatekin. Bilateral Renal Agenesis and Aortic Stenosis in an Antenatally Diagnosed Turner Syndrome. Zeynep Kamil Med J. 2016; 47(4): 128-131

Corresponding Author: Handan Hakyemez Toptan, Türkiye
Manuscript Language: English
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