Results 111 to 120 of about 27,709 (227)

Recurrent Hypoglycaemia Leading to Early Diagnosis of Septo‐Optic Dysplasia in a Small‐for‐Gestational‐Age Infant—A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT Septo‐optic dysplasia (SOD) is a rare condition with highly heterogenous clinical manifestations and can be a diagnostic challenge. It can present with pituitary hormone deficiencies, growth failure, visual impairment, and neurological symptoms. SOD can be diagnosed at different time points—from the prenatal period to childhood. Our team cared
Yuan Rui Leon Tan   +4 more
wiley   +1 more source

Progressive familial intrahepatic cholestasis with normal GGT level appearing with lichenification and enlargement of hands and feet

open access: yesThe Turkish Journal of Pediatrics, 2005
Progressive familial intrahepatic cholestasis is a serious disease of the liver, known as Byler disease, characterized by hepatocellular cholestasis.
Tümay Doğanci   +2 more
doaj  

Bile salt export pump deficiency disease: two novel, late onset, ABCB11 mutations identified by next generation sequencing

open access: yesAnnals of Hepatology, 2016
Progressive familial intrahepatic cholestasis (PFIC) is a heterogeneous group of autosomal recessive cholestatic diseases of childhood and represents the main indication for liver transplantation at this age; PFIC2 involves ABCB11 gene, that encodes the ...
Giovanni Vitale   +8 more
doaj   +1 more source

How to Better Assess the Real Role of the Environment in Pregnancy, From Past to Future: A Relational Open Data Infrastructure Covering 30,000 Births

open access: yesHealth Science Reports, Volume 9, Issue 2, February 2026.
ABSTRACT Background and Aims One of today's challenges in terms of understanding the real impact of the environment on pregnancy and its complications is the ability to work with real‐life data that are correctly and extensively connected to data on the contamination of living environments and individualized exposures.
Sophie Cot   +6 more
wiley   +1 more source

Clinical aspects of pregnancy and childbirth in women with intrahepatic cholestasis of pregnancy

open access: yesOne Health & Risk Management
Introduction. Intrahepatic cholestasis of pregnancy (ICP) is a liver pathology that has negative impact on progression of pregnancy and childbirth in affected women.
Maria CEMORTAN   +3 more
doaj   +1 more source

Genetics and Molecular Modeling of New Mutations of Familial Intrahepatic Cholestasis in a Single Italian Center.

open access: yesPLoS ONE, 2015
Familial intrahepatic cholestases (FICs) are a heterogeneous group of autosomal recessive disorders of childhood that disrupt bile formation and present with cholestasis of hepatocellular origin.
Isabella Giovannoni   +5 more
doaj   +1 more source

Ursodeoxycholic acid therapy in children with cholestatic liver disease

open access: yesThe Turkish Journal of Pediatrics, 1999
The beneficial effect of ursodeoxycholic acid have been documented in adults but experience with this agent is limited in the pediatric population. The objective of this study was to evaluate ursodeoxycholic acid treatment in children with cholestatic ...
Gönül Dinler   +4 more
doaj   +1 more source

Molecular mechanisms for fetal cardiac arrhythmia in intrahepatic cholestasis of pregnancy

open access: yes, 2010
Intrahepatic cholestasis in pregnancy (ICP) is characterized by raised serum bile acids which can cause fetal complications, including preterm labour and intrauterine death. The fetal death in ICP is not well understood. In this thesis, the mechanisms of
Sheikh Abdul Kadir, Siti Hamimah   +1 more
core   +1 more source

Hepatopulmonary syndrome in children and adolescents with portal hypertension in Brazil: A multicenter study

open access: yesJournal of Pediatric Gastroenterology and Nutrition, Volume 82, Issue 2, Page 366-373, February 2026.
Abstract Objectives To describe the clinical and laboratory characteristics and outcomes of pediatric hepatopulmonary syndrome (HPS) secondary to portal hypertension (PH) in Brazil. Methods Fifty‐four pediatric patients diagnosed with PH and HPS according to the European Respiratory Society criteria were included in this multicenter retrospective study.
Leticia Drumond Alberto   +14 more
wiley   +1 more source

Progressive familial intrahepatic cholestasis type 4: a case report

open access: yesJournal of Medical Case Reports
Background Progressive familial intrahepatic cholestasis is an autosomal recessive genetic disorder that manifests primarily with jaundice and pruritus and can progresses from persistent cholestasis to cirrhosis and late childhood liver failure ...
Mohamed Abdelmalak Abokandil   +6 more
doaj   +1 more source

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