Results 151 to 160 of about 2,122 (197)

Serum Dehydroepiandrosterone Sulfate Levels and Pubarche in Short Children Born Small for Gestational Age before and during Growth Hormone Treatment [PDF]

open access: yesJournal of Clinical Endocrinology and Metabolism, 2004
It has been suggested that the programming of the endocrine axes occurs during critical phases of fetal development and will be affected by intrauterine growth retardation.
Paul Mulder   +2 more
exaly   +3 more sources

The prevalence and risk factors of premature thelarche and pubarche in 4- to 8-year-old girls

open access: yesActa Paediatrica, International Journal of Paediatrics, 2012
Aim: To assess the prevalence of premature thelarche (PT) and pubarche in healthy 4- to 8-year-old girls and to investigate factors associated with early pubertal development.
Zeynep Atay   +2 more
exaly   +2 more sources
Some of the next articles are maybe not open access.

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Premature Pubarche

Endocrinology and Metabolism Clinics of North America
Paul Kaplowitz
exaly   +2 more sources

Premature Pubarche: Time to Revise the Diagnostic Approach?

open access: yesJournal of Clinical Medicine, 2023
Premature pubarche (PP) could represent the first manifestation of non-classic congenital adrenal hyperplasia caused by 21 hydroxylase deficiency (NC21OHD) (10–30% of cases).
Rita Ortolano   +2 more
exaly   +2 more sources

Isolated precocious pubarche: an approach.

The Journal of Clinical Endocrinology & Metabolism, 1994
Precocious pubarche (PP) is most often a benign condition secondary to the early appearance of adrenarche. However, PP may be a manifestation of nonclassical adrenal hyperplasia. The incidence of nonclassical adrenal hyperplasia in patients with PP ranges from about 0-40% of cases. Controversy exists as to whether all children with PP should undergo an
BALDUCCI R   +4 more
openaire   +4 more sources

Premature pubarche: etiological heterogeneity

Journal of Clinical Endocrinology & Metabolism, 1992
Premature pubarche is characterized by pubic hair, adult type body odor, acne, and axillary hair before 8 yr of age in girls and 9.5 yr of age in boys. Causes of this premature virilization include premature adrenarche, mild errors of steroidogenesis, precocious puberty, and adrenal and gonadal tumors.
S F, Siegel   +4 more
openaire   +3 more sources

Genetic Defects of Steroidogenesis in Premature Pubarche*

The Journal of Clinical Endocrinology & Metabolism, 1987
Twenty three patients (19 girls, 4 boys) presented with typical features of premature pubarche between the ages of 2-7 yr. The patients were studied for the presence of an adrenal steroidogenic defect by ACTH stimulation testing (Cortrosyn, 0.25 mg iv bolus dose).
J W, Temeck   +3 more
openaire   +2 more sources

Pronounced Adrenarche and Precocious Pubarche in Boys

Hormone Research in Paediatrics, 1999
In girls, pronounced adrenarche with precocious pubarche (PP) has been related to reduced fetal growth and to a cluster of endocrine-metabolic abnormalities. We examined whether these associations are also evident in boys with PP. The study population consisted of matched groups of boys (n = 58; age range 5–15 years) without or with a history of PP ...
N, Potau   +4 more
openaire   +2 more sources

Premature Pubarche in Children with Pompe Disease

The Journal of Pediatrics, 2015
Pompe disease (PD), or glycogen storage disease type II, results from deficiency of acid α-glucosidase. Patients with infantile-onset PD die by early childhood if untreated. Patient survival has improved with enzyme replacement therapy. We report a case series of 8 patients with infantile-onset PD on enzyme replacement therapy with premature pubarche.
Queenie K-G, Tan   +8 more
openaire   +2 more sources

Natural history of premature pubarche: an auxological study

Journal of Clinical Endocrinology & Metabolism, 1992
The natural history of girls with premature pubarche is reported to be normal, but the effects on puberty and on final height are not well documented. We assessed the outcome of a group of girls with premature pubarche from two Latin populations in whom 21-hydroxylase deficiency had been ruled out by an ACTH test.
L. Ibanez   +8 more
openaire   +4 more sources

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