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Children with premature pubarche: is an alterated neonatal 17-Ohp screening test a predictive factor...

Children with premature pubarche: is an alterated neonatal 17-Ohp screening test a predictive factor...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_2376c08fd05c4c77a0dfe1d79c577e52

Children with premature pubarche: is an alterated neonatal 17-Ohp screening test a predictive factor?

About this item

Full title

Children with premature pubarche: is an alterated neonatal 17-Ohp screening test a predictive factor?

Publisher

England: BioMed Central

Journal title

Italian journal of pediatrics, 2018-01, Vol.44 (1), p.10-10, Article 10

Language

English

Formats

Publication information

Publisher

England: BioMed Central

More information

Scope and Contents

Contents

Neonatal screening for 21 hydroxylase deficiency is designed to detect classical form of congenital adrenal hyperplasia (CAH). It is still unclear whether newborns who result false positives at neonatal screening might later develop signs of androgen excess. The aim of this study is to verify whether a slightly elevated 17-OHP at newborn screening...

Alternative Titles

Full title

Children with premature pubarche: is an alterated neonatal 17-Ohp screening test a predictive factor?

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_2376c08fd05c4c77a0dfe1d79c577e52

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_2376c08fd05c4c77a0dfe1d79c577e52

Other Identifiers

ISSN

1824-7288

E-ISSN

1824-7288

DOI

10.1186/s13052-018-0444-6

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