A rare combination: congenital adrenal hyperplasia due to 21 hydroxylase deficiency and Turner syndrome

A combination of Turner syndrome (TS) and classical congenital adrenal hyperplasia (CAH) is rare. A one-day-old newborn was referred to our hospital with ambiguous genitalia. The parents were third-degree relatives. The infant's weight was 3350g (50-75p), and the head circumference was 34.5cm (...

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Veröffentlicht in:	Journal of clinical research in pediatric endocrinology 2012-12, Vol.4 (4), p.213-215
Hauptverfasser:	Kendirci, Havva Nur Peltek, Aycan, Zehra, Çetinkaya, Semra, Baş, Veysel Nijat, Ağladıoğlu, Sebahat Yılmaz, Önder, Aşan
Format:	Artikel
Sprache:	eng
Schlagworte:	Adrenal Hyperplasia, Congenital - complications Adrenal Hyperplasia, Congenital - genetics Adrenal Hyperplasia, Congenital - physiopathology Adrenal Hyperplasia, Congenital - therapy Case Report Child Development Consanguinity Disorders of Sex Development - etiology Female Humans Infant, Newborn Treatment Outcome Turner Syndrome - complications Turner Syndrome - genetics Turner Syndrome - physiopathology Turner Syndrome - therapy
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