hrp0092p3-307 | Late Breaking Abstracts | ESPE2019
Tankoska Maja
, Murtezani Avdi
, Jovanovska Anamarija
, Miladinova Daniela
, Kocheva Svetlana
Introduction: Beta thalassemia is a common genetic disorder in Mediterranean countries. Congenital hypothyroidism is also a condition resulting with deficiency of thyroid hormone in newborn infants. Autoimmune thyroid dysfunction in childhood patients with thalassemia major is uncommon and poorly described. We report a case of a child with two independent diseases - clinical hypothyroidism diagnosed in early childhood, and beta thalassemia major who developed ...