ea0029p1108 | Neuroendocrinology | ICEECE2012
Bonomi M.
, Libri D.
, Pincelli A.
, Guizzardi F.
, Maiolo E.
, Maghnie M.
, Krausz C.
, Persani L.
, On behalf of the Italian Network for ICH
Introduction: ICH is a rare and heterogeneous condition due to defects of GnRH secretion or action. Recent data indicate that ICH, though characterized by a strong genetic component, is a disease of multifactorial origin. Indeed, digenic defects have been described as a possible pathogenic explanation for ICH.Subjects: We present two familial cases with particular clinical and genetic profiles, out of a cohort of 300 ICH patients.R...