Septo-optic dysplasia (SOD) is a rare congenital disease that has been
described in association with hypothalamic dysfunction. A case of pol
yendocrine dysfunction is described in a 22 year-old white female with
septo-optic dysplasia. Findings included atrophic optic nerves, a cav
um septum pellucidum and a small pituitary gland detected by magnetic
resonance imaging. The patient had central diabetes insipidus, Hashimo
to's thyroiditis, and gestational diabetes mellitus. A review of the l
iterature is presented. A careful and detailed endocrine evaluation is
needed in patients with SOD.