Results 51 to 60 of about 5,099,040 (214)
Turner Syndrome; A Case Report With Growth Failure
Turner syndrome which afflicts approximately 50 per 100000 females is characterized by retarded growth, gonadal dysgenesis, and infertility. Growth failure is a consistent finding at birth in infants with Turner's syndrome.
Betül Ersoy +3 more
doaj +2 more sources
Automated cTDI in sheep fetuses provided reproducible measurements of myocardial velocities and heart rate that align well with manual pulsed‐wave TDI. For cardiac cycle duration metrics, the two modalities are not interchangeable. These findings support that automated cTDI is well suited for longitudinal assessment under both physiological and ...
Juulia Lantto +6 more
wiley +1 more source
Objectives: To study the maternal determinants of intrauterine growth retardation among cases admitted for delivery in Bundelkhand Medical College, Sagar.
Shikha Pandey , Ramesh Pandey
doaj
Clinical features of pneumocystic pneumonia in newborns [PDF]
The research goal is to study clinical features and incidence of pneumocystic pneumonia in newborns. The research methods: The research has included 227 newborns with pneumocystic pneumonia: 154 (67,8%) — premature, 64 (28,1 %) — mature with intrauterine
Gasanova T.A. +2 more
doaj
Trained Immunity in Childhood Vaccination
Trained immunity as an emerging concept in paediatric vaccinology. Trained immunity links vaccine stimuli through epigenetic and metabolic reprogramming to enhanced innate immune cell function, thereby strengthening protection against diverse pathogens while promoting adaptive immune responses through more efficient antigen presentation and co ...
ChenRongRong Cai +2 more
wiley +1 more source
Retardo del crecimiento intrauterino Intrauterine growth retardation
<p class="MsoNormal"><span style="font-size: 9pt; font-family: Arial">El crecimiento fetal anormal es un aspecto de gran interés en la obstetricia actual y un dilema clínico relativamente frecuente.
Adriana Cuartas Calle
doaj
A New Case of Lethal Congenital Contracture Syndrome Type 3 With Hyperinsulinism and Optic Atrophy
PIP5K1C‐related lethal congenital contracture syndrome with hyperinsulinism and optic atrophy. ABSTRACT Lethal congenital contracture syndrome 3 (LCCS3, MIM #611369) is a rare autosomal recessive neuromuscular disorder caused by biallelic loss‐of‐function (LOF) variants in PIP5K1C, reported in only two families to date.
Tameemi Abdalla Moady +3 more
wiley +1 more source
Abstract Aim To characterize reported perinatal complications and childhood neurological diagnoses among children with COL4A1/2 variants and explore associations between mode of delivery and selected neurological outcomes. Method This was a retrospective cross‐sectional patient registry study using surveys collected through the Gould Syndrome ...
Shraddha Pandey +3 more
wiley +1 more source
Excavation at University College London revealed more than 8700 human skeletal fragments representing at least 38 individuals, alongside over 800 animal remains. Features consistent with dissection, specimen preparation and curation provide evidence for the use of human and animal material in nineteenth‐century anatomical education, offering rare ...
Wendy Birch, Tania Kausmally
wiley +1 more source
Intrauterine growth retardation (IUGR / SGA) - causes, clinical view, consequences [PDF]
Deficient intrauterine growth may point to a serious health problem of fetus. It is associated with increased perinatal and neonatal mortality and morbidity. Long-term health consequences have been reported in IUGR / SGA children.
Kročilová, Kateřina
core

