Searchable abstracts of presentations at key conferences in endocrinology

ea0022p641 | Neuroendocrinology and Pituitary (<emphasis role="italic">Generously supported by Novartis</emphasis>) | ECE2010

Heterogeneous origin of idiopathic isolated central hypothyroidism

Bonomi Marco , Libri Domenico Vladimiro , De Filippis Tiziana , Maggi Mario , Pilotta Alba , De Bellis Annamaria , Salvatoni Alessandro , Buzi Fabio , Beck-Peccoz Paolo , Nespoli Luigi , Persani Luca

Isolated central hypothyroidism (ICH) is a rare disease whose pathogenesis is so far linked to germinal mutations of TSHβ (several cases) or TRH receptor (TRHR) genes (only two cases). Here, we report the studies performed to elucidate the pathogenesis of idiopathic ICH in five cases (two men, three women) with low/normal TSH levels and low freeT4 levels (3–8 pmol/l). One male, negative at neonatal TSH screening, showed signs of severe hypothyroidism at 44...