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Zeynep Kamil Med J. 2015; 46(4): 118-120 | DOI: 10.16948/zktb.42746
2Zeynep Kamil Gynecology, Child Health and Diseases Education and Res. Hospital. Pediatric Cardiology Clinic, Istanbul
Late Hypocalcemia with Di George Syndrome in a Rare Case of Neonatal Period
Handan Hakyemez Toptan1, Ayşen Akbaş1, Tülin Gökmen Yıldırım1, Taner Yavuz2, Fahri Ovalı1, Güner Karatekin11Zeynep Kamil Gynecology, Child Health and Diseases Eğt. and Res. Hospital Neonatology Clinic, Istanbul2Zeynep Kamil Gynecology, Child Health and Diseases Education and Res. Hospital. Pediatric Cardiology Clinic, Istanbul
Classical triad of DiGeorge Syndrome (DGS), where more than %90 of patients are detected by 22q11 deletion, is formed by congenital heart diseases, large vascular anomalies, palatal incapacity, and hypocalcemia. Hypoplasia of timus, speaking and nutrition problems, and mental retardation are other frequently observed signs. Apart from these, several different phenotypic characteristics are identified
Keywords: DiGeorge syndrome, multicystic kidney, 22q11 deletion syndrome, hypocalcemiaHandan Hakyemez Toptan, Ayşen Akbaş, Tülin Gökmen Yıldırım, Taner Yavuz, Fahri Ovalı, Güner Karatekin. Late Hypocalcemia with Di George Syndrome in a Rare Case of Neonatal Period. Zeynep Kamil Med J. 2015; 46(4): 118-120
Corresponding Author: Handan Hakyemez Toptan, Türkiye
Manuscript Language: English
Corresponding Author: Handan Hakyemez Toptan, Türkiye
Manuscript Language: English
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