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Hypertransaminasemia children

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https://www.readbyqxmd.com/read/27548248/hypertransaminasemia-in-newly-diagnosed-pediatric-patients-with-celiac-disease
#1
Grace J Lee, Brendan Boyle, Tracy Ediger, Ivor Hill
OBJECTIVES: The aim of the present study was to determine the proportion of pediatric patients with celiac disease (CD) who had transaminases obtained at diagnosis and to determine the proportion with hypertransaminasemia. METHODS: Data from newly diagnosed patients with CD at Nationwide Children's Hospital from February 2007 to March 2014 were retrospectively reviewed. Alanine transaminase (ALT) and aspartate transaminase (AST) values at diagnosis and after initiation of a gluten-free diet (GFD) were assessed...
September 2016: Journal of Pediatric Gastroenterology and Nutrition
https://www.readbyqxmd.com/read/26894285/the-etiology-of-hypertransaminasemia-in-turkish-children
#2
Filiz Serdaroğlu, Tuğba Koca, Selim Dereci, Mustafa Akçam
The aim of this study was to investigate the causes of elevated levels of alanine aminotransferase (ALT) and aspartate aminotransferase (AST) in children. We analyzed the medical records for children aged 3 months to 18 years who presented to the hospital with ALT >45 IU/L and/or AST >50 IU/L, between 2012 and 2014, for various reasons, including those not related to liver disease. In total, 281 children met the study criteria. This group comprised of 125 (44.5%) females and 156 (55.5%) males. At the presentation, the most common patient complaint was fatigue (53...
2016: Bosnian Journal of Basic Medical Sciences
https://www.readbyqxmd.com/read/25518532/alpha-1-antitrypsin-deficiency-in-children-clinical-characteristics-and-diagnosis
#3
Nedeljko Radlović, Zoran Leković, Vladimir Radlović, Dušica Simić, Aleksandra Topić, Dragana Ristić, Siniša Dučić, Andjelo Beletić, Andjelo Baletić
INTRODUCTION: Alpha-1-antitrypsin deficiency (AATD) is a relatively rare and clinically very heterogeneous autosomal recessive disorder. OBJECTIVE: Presentation of clinical characteristics of AATD in the first months after birth, as well as the significance of testing brothers and sisters for its presence. METHODS: Objectives of the study were analyzed on a sample of eight children (four male and four female, aged 63 months (mean 14.81 ± 23...
September 2014: Srpski Arhiv za Celokupno Lekarstvo
https://www.readbyqxmd.com/read/25439061/from-hypertransaminasemia-to-mucopolysaccharidosis-iiia
#4
Paulina Krawiec, Elżbieta Pac-Kożuchowska, Beata Mełges, Agnieszka Mroczkowska-Juchkiewicz, Stanisław Skomra, Agnieszka Pawłowska-Kamieniak, Katarzyna Kominek
UNLABELLED: ᅟ: Mucopolysaccharidosis type III (MPS III; Sanfilippo syndrome) is a metabolic disorder characterized by the deficiency of a lysosomal enzyme catalyzing the catabolic pathway of heparan sulphate. MPS III presents with progressive mental deterioration, speech delay and behavioural problems with subtle somatic features, which can often lead to misdiagnosis with idiopathic developmental/speech delay, attention deficit/hyperactivity disorder or autism. We report a case of a 5-year-old boy with developmental delay and behaviour problems admitted to the Department of Paediatrics due to chronic hypertransaminasemia...
2014: Italian Journal of Pediatrics
https://www.readbyqxmd.com/read/24285451/clinical-picture-of-classical-atypical-and-silent-celiac-disease-in-children-and-adolescents
#5
Barbara Iwańczak, Krzysztof Matusiewicz, Franciszek Iwańczak
BACKGROUND: Celiac disease is a frequent disease of the alimentary tract in children. Clinical presentation of the disease is variable and depends on type of the disease. OBJECTIVES: The aim of the study was an analysis of clinical findings, selected laboratory features and coexisting diseases in children and adolescents with celiac disease. MATERIAL AND METHODS: Material of the study comprised a series of 78 children aged 8 months - 13 years...
September 2013: Advances in Clinical and Experimental Medicine: Official Organ Wroclaw Medical University
https://www.readbyqxmd.com/read/23687411/persistent-hypertransaminasemia-in-asymptomatic-children-a-stepwise-approach
#6
REVIEW
Pietro Vajro, Sergio Maddaluno, Claudio Veropalumbo
We aimed to examine the major causes of isolated chronic hypertransaminasemia in asymptomatic children and develop a comprehensive diagnostic flow diagram. A MEDLINE search inclusive of publications throughout August 2012 was performed. We found only a small number of publications that had comprehensively investigated this topic. Consequently, it was difficult to construct a diagnostic flowchart similar to those already available for adults. In children, a "retesting panel" prescription, including gamma-glutamyl transpeptidase and creatine kinase in addition to aminotransferases, is considered a reasonable approach for proficiently confirming the persistence of the abnormality, ruling out cholestatic hepatopathies and myopathies, and guiding the subsequent diagnostic steps...
May 14, 2013: World Journal of Gastroenterology: WJG
https://www.readbyqxmd.com/read/23434875/pediatric-celiac-disease-cryptogenic-hypertransaminasemia-and-autoimmune-hepatitis
#7
Pietro Vajro, Giulia Paolella, Giuseppe Maggiore, Giuseppe Giordano
OBJECTIVE: The association between celiac disease (CD) and liver disease in pediatrics is widely recognized, but its prevalence is unknown. This study aims to conduct a systematic review and meta-analysis to evaluate the prevalence of CD in children with cryptogenic persistent hypertransaminasemia (HTS) or autoimmune hepatitis (AIH), and vice versa. METHODS: We searched MEDLINE/PubMed, the Cochrane Library, Web of Science, and MD Consult from 1977 to May 2012 for studies reporting either CD and HTS or AIH...
June 2013: Journal of Pediatric Gastroenterology and Nutrition
https://www.readbyqxmd.com/read/22773723/consider-muscle-disease-in-children-with-elevated-transaminase
#8
Melissa A Wright, Michele L Yang, Julie A Parsons, John M Westfall, Audrey S Yee
The transaminases alanine aminotransferase (ALT) and aspartate aminotransferase (AST) are markers of hepatocellular injury but are highly concentrated in muscle cells. Consequently, muscular dystrophies such as Duchenne muscular dystrophy, lead to hypertransaminasemia. Elevation in ALT and AST is most striking during the early stages of disease, before onset of or when only subtle signs of muscle disease are present. Thus, the incidental finding of elevated ALT/AST may be the presenting sign of muscle disease in many children and provides an opportunity for early diagnosis...
July 2012: Journal of the American Board of Family Medicine: JABFM
https://www.readbyqxmd.com/read/22521558/non-alcoholic-fatty-liver-disease-in-children
#9
Wojciech Janczyk, Piotr Socha
Non-alcoholic fatty liver disease is increasingly prevalent in children, together with obesity. Transaminases, tests for insulin resistance, ultrasonography and MRI are variably used as surrogates markers of steatosis. Other liver diseases, such as Wilson disease, should be excluded. A liver biopsy is performed in selected cases: young children, familial history of severe disease, inconclusive tests for other pathologies, suspected advanced fibrosis, hypertransaminasemia despite weight loss and in clinical trials...
June 2012: Clinics and Research in Hepatology and Gastroenterology
https://www.readbyqxmd.com/read/21505361/effects-of-lactobacillus-rhamnosus-strain-gg-in-pediatric-obesity-related-liver-disease
#10
RANDOMIZED CONTROLLED TRIAL
Pietro Vajro, Claudia Mandato, Maria Rosaria Licenziati, Adriana Franzese, Dino Franco Vitale, Selvaggia Lenta, Maria Caropreso, Gianfranco Vallone, Rosaria Meli
OBJECTIVE: Various lines of evidence suggest that malfunctioning of the gut-liver axis contributes to hepatic damage of rodents and humans with nonalcoholic fatty liver disease. We evaluated the effects of short-term probiotic treatment in children with obesity-related liver disease who were noncompliant with lifestyle interventions. PATIENTS AND METHODS: Twenty obese children (age 10.7 ± 2.1 years) with persisting hypertransaminasemia and ultrasonographic (US) bright liver were enrolled in this double-blind, placebo-controlled pilot study...
June 2011: Journal of Pediatric Gastroenterology and Nutrition
https://www.readbyqxmd.com/read/20601906/transient-hypertransaminasemia-in-paediatric-patients-with-crohn-disease-undergoing-initial-treatment-with-enteral-nutrition
#11
Ellen Schatorjé, Hans Hoekstra
OBJECTIVES: Total enteral nutrition (TEN) is frequently used as monotherapy in children with Crohn disease to prevent steroid toxicity. Liver disease is a known complication in inflammatory bowel disease, and liver enzymes are regularly obtained in these patients. PATIENTS AND METHODS: Prospective follow-up of liver enzymes was performed in 11 new consecutive patients ages 7.6 to 17.1 years who were primarily treated with TEN for 6 weeks. Liver enzymes were measured before starting TEN and after 3, 6, and 12 weeks...
September 2010: Journal of Pediatric Gastroenterology and Nutrition
https://www.readbyqxmd.com/read/20500440/aminotransferases-and-muscular-diseases-a-disregarded-lesson-case-reports-and-review-of-the-literature
#12
REVIEW
Claudio Veropalumbo, Ennio Del Giudice, Gabriella Esposito, Sergio Maddaluno, Lucia Ruggiero, Pietro Vajro
The aim of this study was to call the attention to the often disregarded message that hypertransaminasemia may be a marker of both liver and muscle diseases by presenting personal case reports and a systematic literature review. Three male children (mean age 5.7 years) were inappropriately addressed, during the last 12 months, to our paediatric liver unit for diagnostic work-up of a chronic hypertransaminasemia of unknown origin. In one of them, a liver biopsy had already been performed. On admission, physical examination, evaluation of serum levels of creatine kinase, and dystrophin genetic testing finally led to a diagnosis of muscular dystrophy...
October 2012: Journal of Paediatrics and Child Health
https://www.readbyqxmd.com/read/20422917/coeliac-disease-as-the-cause-of-resistant-sideropenic-anaemia-in-children-with-down-s-syndrome-case-report
#13
Momcilo Pavlović, Nedeljko Radlović, Zoran Leković, Karolina Berenji, Zorica Stojsić, Vladimir Radlović
INTRODUCTION: Coeliac disease (CD) is a permanent intolerance of gluten, i.e., of gliadin and related proteins found in the endosperm of wheat, rye and barley. It is characterized by polygenic predisposition, autoimmune nature, predominantly asymptomatic or atypical clinical course, as well as by high prevalence in patients with Down's syndrome (DS) and some other diseases. OUTLINE OF CASES: We are presenting a girl and two boys, aged 6-7 (x = 6.33) years with DS and CD recognized under the feature of sideropenic anaemia resistant to oral therapy with iron...
January 2010: Srpski Arhiv za Celokupno Lekarstvo
https://www.readbyqxmd.com/read/19362523/elevated-serum-alt-in-children-presenting-to-the-emergency-unit-relationship-with-nafld
#14
V Nobili, A Reale, A Alisi, G Morino, I Trenta, M Pisani, M Marcellini, U Raucci
BACKGROUND: Non-alcoholic fatty liver disease, ranging from hepatic steatosis to necro-inflammation with or without fibrosis (non-alcoholic steatohepatitis), is a growing clinical liver disorder in children. AIM: The goals of this study were to characterize liver disorders associated with elevated aminotransferases and establish the non-alcoholic fatty liver disease/non-alcoholic steatohepatitis prevalence in hypertransaminasemic children admitted to the emergency room...
October 2009: Digestive and Liver Disease
https://www.readbyqxmd.com/read/18702652/age-related-clinical-serological-and-histopathological-features-of-celiac-disease
#15
Santiago Vivas, Jose M Ruiz de Morales, Marisa Fernandez, Mercedes Hernando, Blanca Herrero, Javier Casqueiro, Santiago Gutierrez
BACKGROUND: Celiac disease (CD) is a common disorder in children and adults. However, limited data are available when comparing differences between both populations. AIMS: To prospectively evaluate and compare the clinical and histological features present at diagnosis in a cohort of celiac children and adults. METHODS: Consecutive new cases diagnosed between 2000 and 2006 were prospectively included (66 children and 54 adults). The clinical spectrum was categorized in two groups: (a) typical (malabsorption, chronic diarrhea, or failure to thrive) and (b) oligosymptomatic (abdominal pain, anemia, hypertransaminasemia, or screening in risk groups or in relatives)...
September 2008: American Journal of Gastroenterology
https://www.readbyqxmd.com/read/17111054/gluten-intolerance-sex-and-age-related-features
#16
M J Llorente-Alonso, M J Fernández-Acenero, M Sebastián
OBJECTIVE: Gluten intolerance is an immune-mediated enteropathy associated with gluten-containing foods in genetically susceptible patients. The typical form mainly affecting children shows failure to thrive and/or gastrointestinal symptoms. The adult form is less typical, presenting vague gastrointestinal symptoms, iron deficiency (with or without anemia) or nonspecific serum chemistry abnormalities. The present study aims to analyze clinical and biochemical differences of celiac disease (CD) according to sex and age...
November 2006: Canadian Journal of Gastroenterology, Journal Canadien de Gastroenterologie
https://www.readbyqxmd.com/read/16805911/efficacy-and-tolerability-of-gemtuzumab-ozogamicin-anti-cd33-monoclonal-antibody-cma-676-mylotarg-in-children-with-relapsed-refractory-myeloid-leukemia
#17
MULTICENTER STUDY
Benoit Brethon, Anne Auvrignon, Claire Galambrun, Karima Yakouben, Thierry Leblanc, Yves Bertrand, Guy Leverger, André Baruchel
BACKGROUND: Gemtuzumab ozogamicin (GO) is a cytotoxic anti-CD33 monoclonal antibody that has given promising preliminary results in adult myeloid CD33+ AML. We conducted a retrospective multicenter study of 12 children treated with GO on a compassionate basis (median age 5.5 y). Three patients (2 MDS/AML, 1 JMML) were refractory to first-line treatment, 8 patients with de novo AML were in refractory first relapse, and one patient with de novo AML was in 2nd relapse after stem cell transplantation (SCT)...
2006: BMC Cancer
https://www.readbyqxmd.com/read/16630753/hereditary-fructose-intolerance-and-celiac-disease-a-novel-genetic-association
#18
COMPARATIVE STUDY
Carolina Ciacci, Daniela Gennarelli, Gabriella Esposito, Raffaella Tortora, Francesco Salvatore, Lucia Sacchetti
BACKGROUND & AIMS: Celiac disease (CD) has been associated with several genetic disorders, but has not been associated with hereditary fructose intolerance (HFI). METHODS: We identified CD in 4 female patients affected by HFI from among 38 Italian HFI patients. RESULTS: Three of these patients were children in whom the CD-associated signs were hypertransaminasemia, failure to thrive, low weight, and short stature, whereas the adult patient had protracted diarrhea notwithstanding a fructose-free diet...
May 2006: Clinical Gastroenterology and Hepatology
https://www.readbyqxmd.com/read/16439595/cryptogenic-liver-disease-in-four-children-a-novel-congenital-disorder-of-glycosylation
#19
Claudia Mandato, Lena Brive, Yoshiaki Miura, Joseph Alex Davis, Nicolina Di Cosmo, Stefania Lucariello, Severo Pagliardini, Neung-Seon Seo, Giancarlo Parenti, Raffaella Vecchione, Hudson H Freeze, Pietro Vajro
We investigated the metabolic defect(s) of four children who presented with isolated cryptogenic chronic liver disease, coagulopathy, and abnormalities of several unrelated serum glycoproteins. Analysis of the patients' serum glycoproteins and fibroblasts suggest they have a novel congenital disorder of glycosylation (CDG). All had abnormal transferrin (Tf) isoelectric focusing (IEF) profiles. More detailed analysis of Tf by electrospray ionization mass spectrometry (ESI-MS) showed a plethora of abnormal glycosylations that included loss of 1-2 sialic acids and 1-2 galactose units, typical of Group II defects...
February 2006: Pediatric Research
https://www.readbyqxmd.com/read/16249287/immune-phenotype-and-serum-leptin-in-children-with-obesity-related-liver-disease
#20
Raffaele Iorio, Angela Sepe, Antonietta Giannattasio, Francesco Cirillo, Maria Immacolata Spagnuolo, Adriana Franzese, Silvia Fontana, Daniela Aufiero, Francesco Perna, Angela Vegnente, Giuseppe Matarese
CONTEXT: Little is known about pathogenesis of obesity-related liver disease in childhood. Data on the relationship among leptin, immunological parameters, and liver disease in obese children are lacking. OBJECTIVE: Thus, the objective of this study was to evaluate immune phenotype and leptin serum levels in obese children with and without obesity-related liver disease. DESIGN: The study was performed in two groups of consecutive obese children: the first formed by children with obesity-related liver disease, diagnosed in the presence of chronic hypertransaminasemia, liver steatosis at ultrasound, and absence of known etiologies; the second composed of children with isolated obesity...
January 2006: Journal of Clinical Endocrinology and Metabolism
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