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) identifier identifier identifier

  • 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).