Results 11 to 20 of about 116,093 (277)

CHRONIC CHOLESTASIS IN INFANCY [PDF]

open access: yesRomanian Journal of Pediatrics, 2009
This article focuses on the few disorders that produce chronic cholestasis in infants. The author presents: definition and pathophysiology of cholestasis; the consequences of cholestasis; an approach to diagnosis of cholestasis in infancy and childhood;
Daniela Patrichi
doaj   +1 more source

Neonatal cholestasis as the onset symptom of McCune–Albright syndrome: case reports and a literature review

open access: yesFrontiers in Pediatrics, 2023
AimThis study aimed to summarize and show the characteristics and evolutionary process of neonatal cholestasis caused by McCune–Albright syndrome (MAS), as neonatal cholestasis may be the initial manifestation of MAS before other classic clinical ...
Weiyuan Fang   +3 more
doaj   +1 more source

Biomarkers of Cholestasis [PDF]

open access: yesBiomarkers in Medicine, 2021
Cholestasis is a major pathological manifestation, often resulting in detrimental liver conditions, which occurs in a variety of indications collectively termed cholestatic liver diseases. The frequent asymptomatic character and complexity of cholestasis, together with the lack of a straightforward biomarker, hampers early detection and treatment of ...
Pieters, Alanah   +5 more
openaire   +4 more sources

A meta-analysis of the prevalence of gestational diabetes in patients diagnosed with obstetrical cholestasisAJOG Global Reports at a Glance

open access: yesAJOG Global Reports, 2021
BACKGROUND: Gestational diabetes and obstetrical cholestasis are common clinical conditions seen in clinical practice. There is evidence suggesting a coexisting relationship that could have a potential clinical implication related to stillbirth outcomes.
Manoj Mohan, MRCOG   +3 more
doaj   +1 more source

Neonatal Cholestasis: Updates on Diagnostics, Therapeutics, and Prevention.

open access: yesNeoReviews, 2021
Cholestatic jaundice is a common presenting feature of hepatobiliary and/or metabolic dysfunction in the newborn and young infant. Timely detection of cholestasis, followed by rapid step-wise evaluation to determine the etiology, is crucial to identify ...
Amy G. Feldman, R. Sokol
semanticscholar   +1 more source

Neonatal Cholestasis [PDF]

open access: yesSeminars in Pediatric Surgery, 2000
In simplest terms, cholestasis is defined as a decrease in bile flow. The clinical manifestations of cholestasis occur because of accumulation of substances normally excreted in the bile; namely bilirubin, bile acids, and cholesterol. Accumulation of bilirubin leads to jaundice and dark urine. Accumulation of bile acids is associated with pruritus, and
F M, Karrer, D D, Bensard
openaire   +4 more sources

Re‐evaluating diagnostic thresholds for intrahepatic cholestasis of pregnancy: case–control and cohort study

open access: yesBJOG: an International Journal of Obstetrics and Gynaecology, 2021
To determine the optimal total serum bile acid (TSBA) threshold and sampling time for accurate intrahepatic cholestasis of pregnancy (ICP) diagnosis.
Alice L. Mitchell   +12 more
semanticscholar   +1 more source

The Pathological Mechanisms of Estrogen-Induced Cholestasis: Current Perspectives

open access: yesFrontiers in Pharmacology, 2021
Estrogens are steroid hormones with a wide range of biological activities. The excess of estrogens can lead to decreased bile flow, toxic bile acid (BA) accumulation, subsequently causing intrahepatic cholestasis.
Y. Zu   +3 more
semanticscholar   +1 more source

Distribution of endotoxin in maternal and fetal body with intrahepatic cholestasis of pregnancy and its association with adverse fetal outcome

open access: yesBMC Pregnancy and Childbirth, 2022
Background Intrahepatic cholestasis of pregnancy is a pregnancy-specific liver disease. In this study, we sought to explore the distribution of lipopolysaccharide in the maternal body, and its effect on the fetal body in the intrahepatic cholestasis of ...
Xiaomei Huang   +3 more
doaj   +1 more source

Newer variants of progressive familial intrahepatic cholestasis

open access: yesWorld Journal of Hepatology, 2021
Progressive familial intrahepatic cholestasis (PFIC) is a heterogeneous group of disorders characterized by defects in bile secretion and presentation with intrahepatic cholestasis in infancy or childhood. The most common types include PFIC 1 (deficiency
Vignesh Vinayagamoorthy   +2 more
semanticscholar   +1 more source

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