ea0029p1080 | Neuroendocrinology | ICEECE2012
Maione L.
, Benadjaoud S.
, Ducreux D.
, Sinisi A.
, Chanson P.
, Benoudiba F.
, Young J.
Context: Kallmann syndrome (KS) is a developmental disease associating congenital hypogonadotropic hypogonadism (CHH) and sense of smell impairment owing to olfactory structures (OS) aplasia/hypoplasia. Although rhinencephalic MRI allows to detect specific KS OS abnormalities useful to discriminate KS from normosmic CHH (nCHH), this technique is not efficient enough to study anterior skull bone structures.Objectives: To search for specific anterior skull...