Atıf İçin Kopyala
Karabay N., Comlekci A., Canda M., Bayraktar F., Degirmenci B.
Endocrine journal, cilt.50, sa.4, ss.409-13, 2003 (SCI-Expanded)
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Yayın Türü:
Makale / Tam Makale
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Cilt numarası:
50
Sayı:
4
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Basım Tarihi:
2003
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Doi Numarası:
10.1507/endocrj.50.409
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Dergi Adı:
Endocrine journal
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Derginin Tarandığı İndeksler:
Science Citation Index Expanded (SCI-EXPANDED), Scopus
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Sayfa Sayıları:
ss.409-13
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Anahtar Kelimeler:
thyroid hemiagenesis, nodular goiter, GRAVES-DISEASE, MONOZYGOTIC TWINS, GLAND, DYSGENESIS, HYPERTHYROIDISM, HYPOTHYROIDISM, AGENESIS, ADENOMA, LOBE
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Dokuz Eylül Üniversitesi Adresli:
Evet
Özet
Thyroid hemiagenesis is a very rare abnormality, in which one thyroid lobe fails to develop. Most of the patients diagnosed have an associated thyroidal disease. The true prevalence of thyroid hemiagenesis is not known, but it is estimated to be 0.02% in normal children. We report a forty-five year-old female patient with a multinodular goiter in left lobe, associated with hemiagenesis of right lobe and isthmus.