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Article type: Research Article
Authors: Ozturk, M.A. | Bastug, O. | Halis, H. | Korkmaz, L. | Memur, S. | Sarici, D. | Kara, A.
Affiliations: Erciyes University Medical Faculty, Department of Neonatology, Kayseri, Turkey | Erciyes University Medical Faculty, Department of Pediatrics, Kayseri, Turkey
Note: [] Corresponding author: Dr. Osman Bastug, Division of Neonatology, Department of Pediatrics, Erciyes University Medical Faculty, Talas Street, 38039 Kayseri, Turkey. Tel.: +90 3522076666; Fax: +90 3524375825; E-mail: drosman76@hotmail.com
Abstract: Sirenomelia or the Mermaid syndrome is a rare congenital anomaly with an incidence of one in 60,000 to 70,000 pregnancies. Sirenomelia is characterized by complete fusion of the lower limbs, commonly associated with renal agenesis, absent external genitalia and other gastrointestinal defects. A 37-week, 3040-g infant was born to a 35-year-old multigravida mother with type 2 diabetes mellitus and hyperlipidemia. To our knowledge, this is the first case of sirenomelia with adrenalomegaly.
Keywords: Sirenomelia, adrenalomegaly, infant, diabetes, Mermaid syndrome
DOI: 10.3233/NPM-1476813
Journal: Journal of Neonatal-Perinatal Medicine, vol. 7, no. 3, pp. 253-256, 2014
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