Treatment of Peripheral Precocious Puberty

dc.contributor.authorSchoelwer, Melissa
dc.contributor.authorEugster, Erica A.
dc.contributor.departmentDepartment of Pediatrics, IU School of Medicineen_US
dc.date.accessioned2016-07-13T15:24:15Z
dc.date.available2016-07-13T15:24:15Z
dc.date.issued2016
dc.description.abstractThere are many etiologies of peripheral precocious puberty (PPP) with diverse manifestations resulting from exposure to androgens, estrogens, or both. The clinical presentation depends on the underlying process and may be acute or gradual. The primary goals of therapy are to halt pubertal development and restore sex steroids to prepubertal values. Attenuation of linear growth velocity and rate of skeletal maturation in order to maximize height potential are additional considerations for many patients. McCune-Albright syndrome (MAS) and familial male-limited precocious puberty (FMPP) represent rare causes of PPP that arise from activating mutations in GNAS1 and the LH receptor gene, respectively. Several different therapeutic approaches have been investigated for both conditions with variable success. Experience to date suggests that the ideal therapy for precocious puberty secondary to MAS in girls remains elusive. In contrast, while the number of treated patients remains small, several successful therapeutic options for FMPP are available.en_US
dc.eprint.versionAuthor's manuscripten_US
dc.identifier.citationSchoelwer, M., & Eugster, E. A. (2016). Treatment of Peripheral Precocious Puberty. In Puberty from Bench to Clinic (Vol. 29, pp. 230-239). Karger Publishers. http://dx.doi.org/10.1159/000438895en_US
dc.identifier.urihttps://hdl.handle.net/1805/10368
dc.language.isoenen_US
dc.publisherKargeren_US
dc.relation.isversionof10.1159/000438895en_US
dc.relation.journalPuberty from Bench to Clinicen_US
dc.rightsPublisher Policyen_US
dc.sourceAuthoren_US
dc.subjectperipheral precocious pubertyen_US
dc.titleTreatment of Peripheral Precocious Pubertyen_US
dc.typeArticleen_US
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