Final Diagnosis in Children with Subclinical Hypothyroidism and Mutation Analysis of the Thyroid Peroxidase Gene (TPO)

TURKKAHRAMAN, Doga; Alper, ÖZGÜL; AYDIN, FUNDA; YILDIZ, Akin; Pehlivanoglu, SURAY; LULECI, Guven; Akcurin, SEMA; Bircan, İFFET

doi:10.1515/jpem.2009.22.9.845

Final Diagnosis in Children with Subclinical Hypothyroidism and Mutation Analysis of the Thyroid Peroxidase Gene (TPO)

TURKKAHRAMAN D., Alper O. M., AYDIN F., YILDIZ A., Pehlivanoglu S., LULECI G., ...Daha Fazla

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, cilt.22, sa.9, ss.845-851, 2009 (SCI-Expanded, Scopus)

Yayın Türü: Makale / Tam Makale
Cilt numarası: 22 Sayı: 9
Basım Tarihi: 2009
Doi Numarası: 10.1515/jpem.2009.22.9.845
Dergi Adı: JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
Sayfa Sayıları: ss.845-851
Anahtar Kelimeler: subclinical hypothyroidism, TPO gene, perchlorate discharge test, IODIDE ORGANIFICATION DEFECT, CONGENITAL HYPOTHYROIDISM, GOITROUS HYPOTHYROIDISM, INACTIVATING MUTATIONS, HIGH PREVALENCE
Akdeniz Üniversitesi Adresli: Evet

Özet

Aim: To determine the final diagnosis of patients with subclinical hypothyroidism (SCH), and to perform mutation screening of the thyroid peroxidase gene (TPO).