hrp0082p2-d1-590 | Thyroid | ESPE2014

Thyroid Disorders in Siblings of CH Patients with Thyroid Dysgenesis

Cassio Alessandra , Ruscio Valentina Di , Baronio Federico , Bettocchi Ilaria , Cantasano Antonella , Bal Milva Orquidea , Balsamo Antonio , Maltoni Giulio , Mazzanti Laura

Background: Thyroid dysgenesis has been considered a sporadic disease, but recent observations suggested a possible genetic basis.Objective and hypotheses: The aim of our report is to evaluate the incidence of hormonal and ultrasound thyroid anomalies in siblings of CH patients with thyroid dysgenesis.Method: In Emilia-Romagna Region (Italy) 328 CH infants were diagnosed by neonatal screening between January 2000 and December 2012....