Results 31 to 40 of about 1,240 (130)

Puberty in girls with Prader-Willi syndrome: cohort evaluation and clinical recommendations in a Latin American tertiary center

open access: yesFrontiers in Endocrinology
IntroductionPrader-Willi syndrome (PWS) is a genetic disorder characterized by hypothalamic-pituitary deficiencies including hypogonadism. In girls with PWS, hypogonadism can present early in childhood, leading to genital hypoplasia, delayed puberty ...
Caroline Gouveia Buff Passone   +10 more
doaj   +1 more source

Review of the Literature on Current Changes in the Timing of Pubertal Development and the Incomplete Forms of Early Puberty

open access: yesFrontiers in Pediatrics, 2019
Puberty is a sensitive period of life characterized by the appearance of secondary sex characteristics which leads to a complete sexual maturation. It physiologically starts between the age of 8 and 13 years in girls and 9 and 14 years in boys.
Giovanni Farello   +4 more
doaj   +1 more source

The Androstenedione Roche Elecsys immunoassay has superior comparability to the LC-MS/MS assay than the Siemens Immulite immunoassay

open access: yesPractical Laboratory Medicine, 2022
Androstenedione (ASD) is a biomarker used in the diagnostic workup of hyperandrogenism, congenital adrenal hyperplasia, premature adrenarche, and polycystic ovary syndrome (PCOS).
Ruhan Wei   +4 more
doaj   +1 more source

Differences in Endocrine Parameters and Psychopathology in Girls with Premature Adrenarche versus On-time Adrenarche [PDF]

open access: yesJournal of Pediatric Endocrinology and Metabolism, 2008
Girls with premature adrenarche (PA) are at risk for multiple problems related to exaggerated androgen synthesis. Whether PA carries a risk of psychopathology remains unknown. This study examined group differences in: (a) anthropometric and endocrine parameters, and (b) mood and behavior problems, in 6-8 year-old girls with PA (n = 40) compared to on ...
Lorah D, Dorn   +6 more
openaire   +2 more sources

Precocious Puberty and Benign Variants in Female Children: Etiology, Diagnostic Challenges, and Clinical Management

open access: yesEndocrines
Precocious puberty, defined as the onset of secondary sexual characteristics before age 8 in girls, presents a diagnostic challenge in distinguishing between normal variants and pathological conditions requiring intervention.
Roberto Paparella   +7 more
doaj   +1 more source

Blood Erythrocyte and Hemoglobin Concentrations in Premature Adrenarche [PDF]

open access: yesThe Journal of Clinical Endocrinology & Metabolism, 2013
Premature adrenarche (PA) is characterized by an earlier than normal increase in adrenocortical androgen production, and it is associated with increased serum IGF-I concentrations. Both the GH-IGF system and androgens, particularly testosterone, are known to enhance erythropoiesis.Our objective was to test the hypothesis that blood erythrocyte count ...
Jääskeläinen Jarmo   +2 more
openaire   +2 more sources

Androgen producing oncocytic adrenocortical tumor in a 3.7-year-old female

open access: yesEndocrinology, Diabetes & Metabolism Case Reports
We report a 3.7-year-old female who presented with clinical features of premature adrenarche. Workup revealed significantly elevated androgen levels and advanced bone maturation, prompting abdominal imaging that identified a 6.0 cm adrenal mass.
Kelli D Mans   +3 more
doaj   +1 more source

Circulating TNF-alpha and IL-6 concentrations and TNF-alpha -308 G>A polymorphism in children with premature adrenarche

open access: yesFrontiers in Endocrinology, 2010
Premature adrenarche (PA), the early rise in adrenal androgen production leading to prepubertal signs of androgen action, has been connected with adverse metabolic features.
Pauliina eUtriainen   +5 more
doaj   +1 more source

The aetiology of extreme tall stature in a screened Finnish paediatric population

open access: yesEClinicalMedicine, 2021
: Background: Extremely tall children (defined as height SDS (HSDS) ≥+3) are frequently referred to specialized healthcare for diagnostic work-up. However, no systematic studies focusing on such children currently exist.
Juho Kärkinen, MD   +4 more
doaj   +1 more source

Is basal serum 17-OH progesterone a reliable parameter to predict nonclassical congenital adrenal hyperplasia in premature adrenarche?

open access: yesThe Turkish Journal of Pediatrics, 2011
To determine the critical features for the diagnosis of nonclassical 21 hydroxylase deficiency (NC210HD) without performing adrenocorticotropic hormone (ACTH) test, we studied 186 cases with premature adrenarche.
E Nazli Gönç   +5 more
doaj  

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