Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Premature adrenarche.

Archives of disease in childhood - 1 Mar 2012

Williams Rachel M, Ward Caleb E, Hughes Ieuan A

Abstract excerpt

Premature adrenarche refers to the presence of secondary sexual hair in girls younger than 8 years old and boys younger than 9 years old. It is a relatively common presentation to paediatricians and is more frequent in girls than boys. It is a benign diagnosis, but other causes of androgen excess such as congenital adrenal hyperplasia or adrenal tumours should be excluded first. In conjunction with history and...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Algorithms
Share to Birth Weight
Share to Child

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Predisposition to Disease

Share to Infant, Newborn

Share to Physical Examination

Share to Polycystic Ovary Syndrome

Share to Puberty, Precocious

Source

Identifiers

PMID: 21835833
DOI: 10.1136/archdischild-2011-300011

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Premature adrenarche.PMID 21835833Read ↗

Premature adrenarche--normal variant or forerunner of adult disease?Semantic proximity Read ↗

History of Polycystic Ovary Syndrome, Premature Adrenarche, and Hyperandrogenism in Pediatric EndocrinologySemantic proximity Read ↗

Continuum of phenotypes and sympathoadrenal function in premature adrenarche.Semantic proximity Read ↗

Clinical review 148: Monogenic disorders of puberty.Semantic proximity Read ↗

Update on the etiology, diagnosis and therapeutic management of sexual precocity.Semantic proximity Read ↗

A rare cause of delayed puberty and primary amenorrhea: 17α-hydroxylase enzyme deficiency.Semantic proximity Read ↗

Hyperandrogenism, insulin resistance and acanthosis nigricans (HAIR-AN syndrome): an extreme subphenotype of polycystic ovary syndrome.Semantic proximity Read ↗

Premature thelarche from phenotype to genotype.Semantic proximity Read ↗

Clinical features suggestive of non-classical 21-hydroxylase deficiency in children presenting with precocious pubarche.Semantic proximity Read ↗

Recognizing rare disorders: aromatase deficiency.Semantic proximity Read ↗

Congenital adrenal hyperplasia.Semantic proximity Read ↗

The Endocrine Phenotype Induced by Pediatric Adrenocortical Tumors Is Age- and Sex-Dependent.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.