Results 61 to 70 of about 2,122 (197)

Adrenal Insufficiency Associated Cardiomyopathy, From Molecule to Clinic: A Comprehensive Review

Health Science Reports, Volume 8, Issue 5, May 2025.
ABSTRACT Background and Aim Adrenal insufficiency (AI), the lack of glucocorticoids (GCs) production or function with or without a lack of mineralocorticoids (MCs) and adrenal androgens, can result in uncommon but life‐threatening complications like shock, circulatory failure, syncope, arrhythmias, dilated cardiomyopathy (DCM), and congestive heart ...
Narges Bazgir, Afsaneh Soltani, Zahra Mohajer, Mohammad Amin Khazeei Tabari, Vahid Eslami   +4 more
wiley   +1 more source

Circulating Growth Differentiation Factor 15 (GDF15) in Paediatric Disease: A Systematic Review

Journal of Cachexia, Sarcopenia and Muscle, Volume 16, Issue 2, April 2025.
ABSTRACT Background Growth Differentiation Factor 15 (GDF15), a nonspecific inflammatory marker and member of the TGF‐β superfamily, has a well‐established role in both inflammation and metabolic modulation, but lacks a comprehensive paediatric literature review.
David W. Kronenberger, Teresa A. Zimmers, Rick K. Ralston, Daniel V. Runco   +3 more
wiley   +1 more source

Premature pubarche in Prader-Willi syndrome: Risk factors and consequences.

OBJECTIVES: Children with Prader-Willi Syndrome (PWS) may develop premature pubarche (PP). We investigated the frequency of PP, and its potential precursors and sequelae, in PWS.
Halpin, Kelsee, Griffing, Emily, Lee, Brian R, Paprocki, Emily   +3 more
core   +1 more source

Optimizing care for MRKH patients: From malformation screening to uterus transplantation eligibility

Acta Obstetricia et Gynecologica Scandinavica, Volume 104, Issue 3, Page 514-521, March 2025.
38% of women with MRKH syndrome are inadequately explored for associated malformations. Early assessment of ovarian reserve is necessary at diagnosis in women with MRKH syndrome. MRKH syndrome may have a familial and hereditary dimension. Abstract Introduction Mayer‐Rokitansky‐Küster‐Hauser (MRKH) syndrome with utero‐vaginal aplasia is the most severe ...
Auriane Cospain, Ludivine Dion, Maud Bidet, Krystel Nyangoh Timoh, Chloé Quelin, Isis Carton, Alinoe Lavillaureix, Karine Morcel, Paul Rollier, Laurent Pasquier, Bénédicte Nouyou, Sylvie Odent, Daniel Guerrier, Erika Launay, Marc‐Antoine Belaud Rotureau, Mélanie Fradin, Sylvie Jaillard, Vincent Lavoué   +17 more
wiley   +1 more source

Investigation of early puberty prevalance and time of adding thelarche to pubarche in girls with premature pubarche: Two- year follow-up results

, 2020
Giriş: Prematür pubarş risk faktörleri literatürde sıkça araştırılmakla birlikte, erkence ergenlik ile ilişkili çalışma sayısı oldukça azdır. Bu çalışmada prematür pubarş ile başvuran kız olgularda 'Gerçekten sıklıkla ergenlik erkene kayıyor mu ...
Olgun, Esin Gizem
core  

The Relationship between Type of Consumed Food, Physical Activity and Anthropometric Indicators with Precocious Puberty among 5 -8 Years -Old Girls in Ahwaz, Iran

نشریه پرستاری ایران, 2015
Background & Aims: The mean age of puberty is different from one country to another and the beginning time of puberty is influenced by various factors including environmental and genetic factors.
N Sharifi, SH Najar
doaj  

Associations between birth characteristics, pubertal timing and adult height

Acta Paediatrica, Volume 114, Issue 3, Page 526-535, March 2025.
Abstract Aim This study investigated the association between gestational age and birth size with pubertal timing, measured as peak height velocity, and adult height. Methods This retrospective, population‐based study was conducted in Sweden in 2023. A sub‐group of the 1974 and 1990 GrowUp Gothenburg cohorts was used (n = 4700, 50% males).
Carin Skogastierna, Nazli Kalay, Diana Swolin‐Eide, Anton Holmgren   +3 more
wiley   +1 more source

Premature pubarche and the growth of the trunk in paralysed children

Annals of Human Biology, 1975
In a hospital supervising prolonged orthopaedic treatment of children suffering from neurological affections, isolated premature pubarche appeared very frequently in children suffering from severe paralytic sequelae of acute anterior poliomyelitis.
G, Duval-Beaupère, G, Soulignac
openaire   +2 more sources

A Challenging Case of Congenital Adrenal Hyperplasia Due to CYP11B1 Deficiency With Uncontrolled Hypertension

Case Reports in Endocrinology, Volume 2025, Issue 1, 2025.
Congenital adrenal hyperplasia (CAH) due to 11‐beta‐hydroxylase deficiency (11β‐OHD) is the second most common steroidogenesis impairment in European populations, characterized by hypertension, hypokalemia, infertility, hyperandrogenism, and genital ambiguity in females.
Pierluigi Mazzeo, Filippo Ceccato, Irene Tizianel, Mattia Barbot, Osamu Isozaki   +4 more
wiley   +1 more source

Heterosexual precocity: rare manifestation of virilizing adrenocortical oncocytoma

Annals of Saudi Medicine, 2013
Adrenocortical oncocytomas are extremely rare, and most of the tumors are benign and nonfunctioning. To our knowledge, only 30 cases have been reported in English published studies, and most patients are 40 to 60 years of age.
Sridhar Subbiah, Uma Nahar, Ram Samujh, Anil Bhansali   +3 more
doaj   +1 more source