Results 51 to 60 of about 254 (126)
ABSTRACT Objectives To predict mandibular landmark displacement during pubertal growth using autoregressive models. Materials and Methods The study included 225 subjects with complete cephalometric radiographs from ages 10 to 18. Data were split by subject into training (180; 83 males, 97 females) and test sets (45; 21 males, 24 females).
Abdullah Al Fahad +7 more
wiley +1 more source
Background. Patients with 17α-hydroxylase deficiency (17 OHD) usually present with tall stature and eunuchoid features, rather than growth retardation. However, unlike the classic form of the disease, short stature due to a lack of pubertal growth
Semih Bolu +3 more
doaj +1 more source
Effect of Small‐Quantity Lipid‐Based Nutrient Supplementation on Children's Cortisol Concentration
ABSTRACT This study investigated the role of early‐life nutrition supplementation in regulating the development of hypothalamic‐pituitary‐adrenal (HPA) axis activity, as evidenced by hair cortisol concentration (HCC), in the iLiNS‐DYAD randomized controlled trial in Ghana.
Helena Nti +16 more
wiley +1 more source
ABSTRACT KBG syndrome is a rare autosomal dominant neurodevelopmental disorder caused by ANKRD11 haploinsufficiency and is characterized by short stature, distinctive facial features, intellectual disability or developmental delay, congenital anomalies and skeletal anomalies.
Marit van der Leij +5 more
wiley +1 more source
Purpose To evaluate medieval and postmedieval Dutch skeletal collections for signs of cam impingent. Methods The medieval collections from Alkmaar Paardenmarkt and Klaaskinderkerke and the postmedieval period from Middenbeemster were studied. Standard osteological methods for sex and age estimation were used. From digital photographs of the femora, the
Nouschka Bosch +3 more
wiley +1 more source
Genotype–Phenotype Spectrum of Non‐Syndromic Monogenic Obesity in a National Paediatric Cohort
ABSTRACT Objective Non‐syndromic monogenic obesity, caused by defects in the leptin‐melanocortin pathway, presents with early‐onset severe obesity and hyperphagia, but genotype–phenotype and metabolic correlations across different genetic forms remain unclear.
Ahmet Kahveci +28 more
wiley +1 more source
This report provides three-phase concept for treating skeletal Class III growing patients with severe space deficiency. Three cases are presented.
Hung-Ying Lin +4 more
doaj +1 more source
ABSTRACT A novel AR frameshift mutation (c.2023_2035del) was identified in a 17‐year‐old phenotypic female with Complete Androgen Insensitivity Syndrome (CAIS). This report emphasizes the necessity of molecular characterization and multidisciplinary management to address diagnosis, surgical timing, and psychological well‐being in disorder of sex ...
Maria Francesca Astorino +10 more
wiley +1 more source
Background/Purpose: The age at menarche reflects a pubertal girl's physiologic maturity. The aims of this study were to evaluate the relationship between the age at menarche and skeletal maturation in female orthodontic patients.
Eddie Hsiang-Hua Lai +6 more
doaj +1 more source
All the bedroom's a stage: Reconceptualizing sex as “performance” to sex as “rehearsal”
Abstract In the United States, sex is often spoken about in terms of performance, and naturally invokes language of theatricality. Sexual performance has been used as an umbrella term to refer to sexual satisfaction, behavior, embodiment, and also pathology in terms of conditions such as erectile dysfunction.
Taylor Harmon
wiley +1 more source

