نتایج جستجو برای: severe hyperbilirubinemia

تعداد نتایج: 329746  

Journal: :Pediatrics 2002
S Umit Sarici Murat Yurdakök Muhittin A Serdar Olcay Oran Gülşen Erdem Gülsevin Tekinalp Sule Yiğit

OBJECTIVE In the era of early discharge of newborns from the hospital, newborns with ABO incompatibility are at especially greater risk for developing a subsequent significant hyperbilirubinemia because some of these infants also may present with some degree of ABO isoimmune disease. In this study, we aimed to determine prospectively the critical serum total bilirubin level to predict significa...

Journal: :The Turkish journal of pediatrics 2008
Selahattin Katar Hatice Oztürkmen-Akay Celal Devecioğlu Mustafa Taşkesen

Hyperbilirubinemia is an important health problem in newborns. The most common causes are Rh and ABO incompatibility, hemolytic anemias, enzyme deficiencies, sepsis, hypothyroidism, pyloric stenosis and breast-milk jaundice. Adrenal hemorrhage is a rare cause of hyperbilirubinemia in the neonate. We present a six-day-old newborn with hyperbilirubinemia and suprarenal hematoma who was born at ho...

2015
Andreia Barateiro Shujuan Chen Mei-Fei Yueh Adelaide Fernandes Helena Sofia Domingues João Relvas Olivier Barbier Nghia Nguyen Robert H. Tukey Dora Brites

Bilirubin-induced neurologic dysfunction (BIND) and kernicterus has been used to describe moderate to severe neurologic dysfunction observed in children exposed to excessive levels of total serum bilirubin (TSB) during the neonatal period. Here we use a new mouse model that targets deletion of the Ugt1 locus and the Ugt1a1 gene in liver to promote hyperbilirubinemiainduced seizures and central ...

2014

Background: Many cases of severe neonatal hyperbilirubinemia never have the underlying cause of the jaundice clearly identified. Thus they are said to have ‘idiopathic’ severe neonatal jaundice. However, finding the exact cause, if it is a genetic condition, can enable informed anticipatory guidance regarding future episodes of hemolysis, anemia, or bilirubin cholelithiasis. Objective: ‘Next ge...

Journal: :Neonatology 2014
Robert D Christensen Hassan M Yaish Richard S Lemons

BACKGROUND Many cases of severe neonatal hyperbilirubinemia never have the underlying cause of the jaundice clearly identified. Thus they are said to have 'idiopathic' severe neonatal jaundice. However, finding the exact cause, if it is a genetic condition, can enable informed anticipatory guidance regarding future episodes of hemolysis, anemia, or bilirubin cholelithiasis. OBJECTIVE 'Next ge...

Journal: :international journal of pediatrics 0
hassan boskabadi department of pediatric, associate professor, neonatal research center, mashhad university of medical sciences, mashhad, iran gholamali maamouri department of pediatric, professor of neonatology, mashhad university of medical sciences, mashhad, iran fatemeh khatami department of pediatrics, neonatal research center, mashhad university of medical sciences, mashhad, iran. mohammad ali kiani department of pediatrics, faculty of medicine, mashhad university of medical sciences, mashhad, iran. abbas abdollahi resident of pediatrics, mashhad university of medical sciences, mashhad, iran maryam zakerhamidi department of midwifery, tonekabon branch, islamic azad university, tonekabon, iran.

background: inadequate milk intake during the first year of neonate’s life can result in weight loss, severe hyperbilirubinemia, and sometimes hypernatremia. in this study, we aimed to determine the relationship between neonatal weight loss and hypernatremia in term breastfed infants with idiopathic jaundice, as well as the necessity of sodium concentration measurement in newborns with idiopath...

2017
Eleni Kotsampasakou Sylvia E. Escher Gerhard F. Ecker

Hyperbilirubinemia is a pathological condition, very often indicative of underlying liver condition that is characterized by excessive accumulation of conjugated or unconjugated bilirubin in sinusoidal blood. In literature there are several indications associating the inhibition of the basolateral hepatic transporters Organic anion transporting polypeptide 1B1 and 1B3 (OATP1B1 and 1B3) with hyp...

Journal: :Drug metabolism and pharmacokinetics 2009
Daisuke Kanda Hitoshi Takagi Yasutsugu Kawahara Yutaka Yata Tomofumi Takakusagi Takeshi Hatanaka Teruo Yoshinaga Keigo Iesaki Kenji Kashiwabara Tsugio Higuchi Masatomo Mori Takeshi Hirota Shun Higuchi Ichiro Ieiri

The Dubin-Johnson syndrome (DJS) is an inherited liver disorder characterized by conjugated hyperbilirubinemia and caused by ABCC2 gene mutations resulting in deficiency of multidrug resistance associated-protein 2 (MRP2) function. A 76-year-old woman with serious jaundice was referred to our hospital. She was clinically diagnosed with DJS with hepatic congestion, due to constrictive pericardit...

2016
C. Rinaldi A. Lesmana Waldemar Simandjuntak Laurentius A. Lesmana

the development of complications after procedure, such as age, heart and lung condition, electrolyte imbalance, advanced liver disease, and liver coagulopathy. Obstructive jaundice, especially in patients with high bilirubin level can be more challenging due to the risks of infection and bleeding [3, 4]. Hyperbilirubinemia can lead to hemostasis impairment due to poor absorption of vitamin K. B...

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