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Santral Erken Puberte Gelişen Bir 11-Beta Hidroksilaz Eksikliği Vakası
2009
Journal:  
Türkiye Çocuk Hastalıkları Dergisi
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Abstract:

11b-hydroxylase deficiency is the second most common cause of congenital adrenal hyperplasia (CAH). CAH is an autosomal recessive disorder. In 11b-hydroxylase deficiency, synthesis of cortisol and corticosteron are affected. Ambiguous genitalia, postnatal virilization, and salt retantion are present in the classical form of 11b-hydroxylase deficiency. In this article, a 3 year old 11b-hydroxylase deficient patient who was administered hydrocortisone and developed central precocious puberty in the follow up is decided to be interesting and worthy to be presented

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Türkiye Çocuk Hastalıkları Dergisi

Field :   Sağlık Bilimleri

Journal Type :   Uluslararası

Metrics
Article : 1.046
Cite : 880
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Türkiye Çocuk Hastalıkları Dergisi