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Central precocious puberty in a girl with LEGIUS syndrome: an accidental association?

Central precocious puberty in a girl with LEGIUS syndrome: an accidental association?

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_fe5b5d9758ce4b228cab5fd59d0f13cf

Central precocious puberty in a girl with LEGIUS syndrome: an accidental association?

About this item

Full title

Central precocious puberty in a girl with LEGIUS syndrome: an accidental association?

Publisher

England: BioMed Central

Journal title

Italian journal of pediatrics, 2021-03, Vol.47 (1), p.50-50, Article 50

Language

English

Formats

Publication information

Publisher

England: BioMed Central

More information

Scope and Contents

Contents

Central precocious puberty is a condition characterized by precocious activation of the hypothalamic-pituitary-gonadal axis. It may be idiopathic or secondary to organic causes, including syndromes such as Neurofibromatosis type 1 (NF1).
We presented a girl of 6 years and 10 months with almost 11 café-au-lait skin macules, without other clinical...

Alternative Titles

Full title

Central precocious puberty in a girl with LEGIUS syndrome: an accidental association?

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_fe5b5d9758ce4b228cab5fd59d0f13cf

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_fe5b5d9758ce4b228cab5fd59d0f13cf

Other Identifiers

ISSN

1824-7288,1720-8424

E-ISSN

1824-7288

DOI

10.1186/s13052-021-01004-9

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