Delayed and Precocious Puberty: Genetic Underpinnings and Treatments

dc.contributor.authorGohil, Anisha
dc.contributor.authorEugster, Erica A.
dc.contributor.departmentPediatrics, School of Medicineen_US
dc.date.accessioned2023-04-11T13:25:33Z
dc.date.available2023-04-11T13:25:33Z
dc.date.issued2020-12
dc.description.abstractDelayed puberty may signify a common variation of normal development, or indicate the presence of a pathologic process. Constitutional delay of growth and puberty is a strongly familial type of developmental pattern and accounts for the vast majority of children who are "late bloomers." Individuals with sex chromosomal abnormalities frequently have hypergonadotropic hypogonadism. There are currently 4 known monogenic causes of central precocious puberty. The primary treatment goal in children with hypogonadism is to mimic normal pubertal progression, while the primary aims for the management of precocious puberty are preservation of height potential and prevention of further pubertal development.en_US
dc.eprint.versionAuthor's manuscripten_US
dc.identifier.citationGohil A, Eugster EA. Delayed and Precocious Puberty: Genetic Underpinnings and Treatments. Endocrinol Metab Clin North Am. 2020;49(4):741-757. doi:10.1016/j.ecl.2020.08.002en_US
dc.identifier.urihttps://hdl.handle.net/1805/32329
dc.language.isoen_USen_US
dc.publisherElsevieren_US
dc.relation.isversionof10.1016/j.ecl.2020.08.002en_US
dc.relation.journalEndocrinology and Metabolism Clinicsen_US
dc.rightsPublisher Policyen_US
dc.sourcePMCen_US
dc.subjectCentral precocious pubertyen_US
dc.subjectDelayed pubertyen_US
dc.subjectHypergonadotropic hypogonadismen_US
dc.subjectPeripheral precocious pubertyen_US
dc.titleDelayed and Precocious Puberty: Genetic Underpinnings and Treatmentsen_US
dc.typeArticleen_US
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