ea0029p1103 | Neuroendocrinology | ICEECE2012
Bellastella G.
, Elefante A.
, Palumbo V.
, D'Errico A.
, Napoli M.
, Maione L.
, Visconti D.
, Vargas O.
, Briganti F.
, Brunetti A.
, Sinisi A.
Kallmann syndrome (KS) is characterized by hypogonadotropic hypogonadism and other non-reproductive disorders including smell deficiency due to olfactory bulb developmental abnormalities. The aim of our study was to evaluate retrospectively the role of MRI in patients with clinical diagnosis of KS, searching for any abnormalities of the brain structures involved.Methods: We evaluated 25 KS pts (1432 years, 4F, 21 M). KS cases were classified as hyp...