Results 51 to 60 of about 7,479 (162)
ABSTRACT Background Pneumonia remains a leading cause of morbidity and mortality among children globally, especially in low‐ and middle‐income countries, where poor nutrition and limited access to healthcare increase vulnerability. Vitamin D deficiency is common among children and has emerged as a significant risk factor associated with respiratory ...
Nurshad Ali
wiley +1 more source
Decline in Age of Nutritional Rickets, Need for Routine Vitamin D Supplementation in Young Infants
Objective: To determine the age at the diagnosis of rickets in children in a tertiary care hospital of Karachi and to assess the association of age at the diagnosis of rickets with serum levels of vitamin D.
Ammarah Jamal +3 more
doaj +1 more source
Abstract Congenital bile acid synthesis defects (BASD), the most common of which is 3β‐hydroxy‐Δ5‐C27‐steroid dehydrogenase oxidoreductase (3β‐HSD7) deficiency, are a rare cause of fat‐soluble vitamin malabsorption. We describe a 14‐year‐old girl who presented at 14 months with a left distal femur fracture and failure to thrive.
Samantha Pendleton +6 more
wiley +1 more source
Unusual presentation of vitamin D-dependent rickets type II in a kitten
Case summary A 15-week-old kitten presented with a 1-month history of intermittent generalised tremors and abdominal distension. Hypocalcaemia associated with increased 1,25-vitamin D 3 was consistent with vitamin D 3 -dependent rickets type II. The bone
Florent Duplan, Christina Maunder
doaj +1 more source
ABSTRACT Limited evidence of nutritional deficiencies has been identified in bioarchaeological studies of Native California populations, although isotopic and ethnohistoric research provides evidence of regional, seasonal, and cultural variability in food shortages.
Alyson Caine +3 more
wiley +1 more source
Raquitismo vitamina D dependente tipo II.
Rickets is a rare child disease especially in developed countries. Nutritional rickets remains the most prevalent condition, although congenital forms are well known.
Raquel Santos +4 more
doaj +1 more source
Abstract Carrier screening for genetic conditions performed preconception or during pregnancy allows identification of fetal risk for inherited autosomal recessive and X‐linked conditions. The goal is to identify at‐risk patients/couples and offer them reproductive options such as preimplantation genetic diagnosis, prenatal testing, or targeted newborn
Emily B. Rosenfeld +5 more
wiley +1 more source
A synergistic electron transfer (ET) optimization strategy modulating conformational dynamics, ET pathway, and substrate orientation is proposed for self‐sufficient cytochrome P450s. Guided by this strategy, a P450 variant with improved ET and catalytic efficiency was identified, and the underlying molecular basis was revealed by computational analysis.
Ziqi Liang +9 more
wiley +1 more source
Rickets and other nutritional deficiencies have largely been eradicated in the industrialized world. However, strict adherence to modern diet trends such as veganism may leave individuals vulnerable to nutritional deficiencies if proper supplementation ...
Stacy R. Bedore +6 more
doaj +1 more source
ABSTRACT Objectives The purpose of this study is to conduct a diachronic analysis of cortical bone loss in Barcelona, spanning from the 1st to 18th century CE, assessing the relationship between cortical bone loss and early‐life stressors, as indicated by linear enamel hypoplasia (LEH) across Roman, Late Antiquity, Medieval, and Modern periods and ...
Antony Cevallos +2 more
wiley +1 more source

