Searchable abstracts of presentations at key conferences in endocrinology

ea0022p839 | Thyroid | ECE2010

FOXE1 polyalanine tract (FOXE1-polyA) length polymorphism in patients with thyroid hemiagenesis and subjects with normal thyroid

Szczepanek Ewelina , Ruchala Marek , Kilinska Lidia , Jaroniec Malgorzata , Szaflarski Witold , Zabel Maciej , Sowinski Jerzy

Introduction: Thyroid hemiagenesis (TH) is a rare inborn anomaly presenting as developmental failure of one thyroid lobe. Recent research on the molecular background underlying thyroid dysgenesis have mainly focused on patients with congenital hypothyroidism. In contrast, subjects presenting TH were only sporadically involved. In addition, whether the same factors are responsible for development of TH and other forms of thyroid dysgenesis is still to be elucidated. Recent stud...