Atıf İçin Kopyala
AYCAN Z., Ocal G., BERBEROĞLU M., Cetinkaya E., Adiyaman P., EVLİYAOĞLU S. O.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, cilt.19, sa.3, ss.245-251, 2006 (SCI-Expanded)
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Yayın Türü:
Makale / Tam Makale
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Cilt numarası:
19
Sayı:
3
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Basım Tarihi:
2006
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Doi Numarası:
10.1515/jpem.2006.19.3.245
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Dergi Adı:
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
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Derginin Tarandığı İndeksler:
Science Citation Index Expanded (SCI-EXPANDED), Scopus
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Sayfa Sayıları:
ss.245-251
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Anahtar Kelimeler:
congenital adrenal hyperplasia, height development, 21-HYDROXYLASE DEFICIENCY, THERAPY, HORMONE, CHILDREN, IGF
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Ankara Üniversitesi Adresli:
Evet
Özet
Objective: Long-term replacement treatment with high doses of steroids in congenital adrenal hyperplasia (CAH) is known to have a negative influence on growth. We evaluated the effects of long-term steroid treatment in patients with classical CAH on height development in relation to genetic height potential.