Sections View Full Chapter Figures Tables Videos Annotate Full Chapter Figures Tables Videos Supplementary Content + At a Glance Download Section PDF Listen ++ Disorder characterized by galactorrhea and amenorrhea. + Synonyms and Classification Download Section PDF Listen ++ Amenorrhea-Galactorrhea-Hyperprolactinemia Syndrome. ++ Type I = Chiari-Frommel Syndrome: persistent AGS after giving birth. Type II = Ahumada-Del Castillo Syndrome (Argonz del Castillo-Ahumada Syndrome; Amenorrhea-Galactorrhea FSH Decrease Syndrome; Nonpuerperal Galactorrhea-Amenorrhea Syndrome): AGS not associated with pregnancy. Estrogen deficiency and decreased urinary gonadotropin levels. Type III = Forbes-Albright Syndrome: AGS caused by chromophobe prolactin-producing adenoma of the pituitary. + Genetic Inheritance Download Section PDF Listen ++ Autosomal dominant. + Pathophysiology Download Section PDF Listen ++ Tumors resembling chromophobe adenomas of the pituitary gland with eosinophilic granulation on tetrachrome staining. + Clinical Aspects Download Section PDF Listen ++ Secondary amenorrhea with galactorrhea. Enlargement of the sella turcica. + Anesthetic Considerations Download Section PDF Listen ++ No known specific anesthetic considerations for this syndrome. + References Download Section PDF Listen ++Rimoin DL, Schimke RN: Genetic Disorders of the Endocrine Glands. St. Louis, CV Mosby, 1971.