Publication:
Precocious Puberty in a Girl with Down Syndrome Due to Primary Hypothyroidism

dc.authorscopusid24338698900
dc.authorscopusid8709976000
dc.authorscopusid7102765260
dc.contributor.authorÖzgen, T.
dc.contributor.authorGüven, A.
dc.contributor.authorAydin, Mahmut
dc.date.accessioned2020-06-21T15:06:23Z
dc.date.available2020-06-21T15:06:23Z
dc.date.issued2009
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Özgen] Ilker Tolga, Department of Pediatric Endocrinology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Güven] Ayla, Department of Pediatric Endocrinology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Aydin] Murat, Department of Pediatric Endocrinology, Ondokuz Mayis Üniversitesi, Samsun, Turkeyen_US
dc.description.abstractVan Wyk-Grumbach syndrome is a rare cause of precocious puberty due to hypothyroidism. We report a case of Van Wyk-Grumbach syndrome in a 4.3-year-old female patient with Down syndrome. She was investigated for hematuria for three months before she was referred to our clinic. Physical examination revealed typical morphologic features of Down syndrome and hypothyroidism. Pubertal development stages were: breast at stage III and pubic hair at stage I. In luteinizing hormone releasing hormone (LHRH) stimulation test, peak LH level remained less than 0.1 mIU/ml. Serum estradiol level was 117.7 pg/ml, which was higher than normal for her age (normal range: 2-15 pg/ml). The pelvic ultrasonographic evaluation revealed bilateral multicystic enlarged ovaries. Serum thyroid stimulating hormone (TSH) concentration was higher than 500 μIU/ml and free thyroxin (FT<inf>4</inf>) and free triiodothyronine (FT <inf>3</inf>) levels were as low as 0.4 ng/dl (0.7-1.48) and 1.0 pg/ml (1.71-3.71), respectively. L-thyroxin treatment at a dose of 100 μg/m 2/day was started. Regression in breast development was obtained after one month and her bleeding did not repeat again. In conclusion, urinary and vaginal bleeding in young children must be clearly differentiated, and hypothyroidism must be investigated in children who have precocious puberty.en_US
dc.identifier.endpage383en_US
dc.identifier.issn0041-4301
dc.identifier.issn2791-6421
dc.identifier.issue4en_US
dc.identifier.pmid19950849
dc.identifier.scopus2-s2.0-70649101311
dc.identifier.scopusqualityQ3
dc.identifier.startpage381en_US
dc.identifier.volume51en_US
dc.identifier.wosWOS:000271486400014
dc.identifier.wosqualityQ3
dc.language.isoenen_US
dc.publisherTurkish J Pediatricsen_US
dc.relation.ispartofTurkish Journal of Pediatricsen_US
dc.relation.journalTurkish Journal of Pediatricsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectDown Syndromeen_US
dc.subjectHypothyroidismen_US
dc.subjectPrecocious Pubertyen_US
dc.titlePrecocious Puberty in a Girl with Down Syndrome Due to Primary Hypothyroidismen_US
dc.typeArticleen_US
dspace.entity.typePublication

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