Results 21 to 30 of about 1,234,995 (195)

Characterization of ultrasound and postnatal pathology in fetuses with heterotaxy syndrome

open access: yesFrontiers in Cardiovascular Medicine, 2023
BackgroundTo explore the diagnostic clues and abnormality spectrum of heterotaxy syndrome by prenatal ultrasonography and postnatal verification.MethodsThe prenatal ultrasonic data of 88 heterotaxy syndrome fetuses were analyzed retrospectively as left ...
Qiumei Wu   +11 more
doaj   +1 more source

BILIARY ATRESIA IS ASSOCIATED WITH POLYSPLENIA AND SITUS INVERSUS ON ULTRASOUND, A CASE REPORT STUDY.

open access: yesStudent's Journal of Health Research Africa, 2023
Biliary atresia is a destructive, idiopathic, and inflammatory cholangiopathy that affects intra and extra-hepatic bile ducts leading to fibrosis and obliteration of the biliary tract and development of liver cirrhosis.
Evalyne Tukwasibwe   +3 more
doaj   +1 more source

Asplenia and spleen hypofunction

open access: yes, 2022
Asplenia (the congenital or acquired absence of the spleen) and hyposplenism (defective spleen function) are common causes of morbidity and mortality. The spleen is a secondary lymphoid organ that is responsible for the regulation of immune responses and
Luu, Sarah   +10 more
core   +2 more sources

Anesthetic Considerations for Non-Cardiac Surgery in an Adult Patient with Right Atrial Isomerism

open access: yesGraduate Medical Education Research Journal, 2021
Mentor: Rebecca Aron Program: Department of Anesthesiology Type: Case Report Background: HS has an estimated incidence of 1 in 6000 to 1 in 20000 live births.
Sagar Bansal, Rebecca Aron
doaj   +1 more source

Isolated congenital asplenia: An overlooked cause of thrombocytosis

open access: yes, 2022
Isolated congenital asplenia: An overlooked cause of ...
Boisson B   +12 more
core   +1 more source

Childhood Morgagni hernia: report of two cases

open access: yesJournal of Pediatric and Neonatal Individualized Medicine, 2017
Morgagni diaphragmatic hernia is a rare congenital anomaly to be seen in the pediatric age group. We are reporting two cases of Morgagni hernia, which presented with non-specific symptoms and posed a diagnostic dilemma.
Kamal Nain Rattan   +2 more
doaj   +1 more source

Syndrome of right isomerism: Ivemark syndrome

open access: yesJournal of Mahatma Gandhi Institute of Medical Sciences, 2018
Heterotaxy Syndrome is a complex syndrome that occurs when the axes of the body fail to rotate correctly when developing in the uterus. This can result in many different organ systems being affected.
Dipti Jain, Bhushan Chavan, Anita Manoj
doaj   +1 more source

Chest radiographic findings in children with asplenia syndrome

open access: yes, 2010
Background: Early diagnosis of asplenia syndrome is important because prophylactic antibiotic and proper vaccination will prevent serious infection. Most children with asplenia syndrome present with symptoms of congenital heart disease.
Kullana Tantiprawan   +2 more
core   +1 more source

Streptococcus pneumoniae and Its Virulence Factors H2O2 and Pneumolysin Are Potent Mediators of the Acute Chest Syndrome in Sickle Cell Disease

open access: yesToxins, 2021
Sickle cell disease (SCD) is one of the most common autosomal recessive disorders in the world. Due to functional asplenia, a dysfunctional antibody response, antibiotic drug resistance and poor response to immunization, SCD patients have impaired ...
Joyce Gonzales   +6 more
doaj   +1 more source

4. Database of dextrocardiac patients in KFSH & RC: Retrospective analysis of 360 patients over the past 20 years

open access: yesJournal of the Saudi Heart Association, 2017
Clinical research. Presentation Type: Oral Presentation Introduction: Dextrocardia is the right-sided positioning of the human heart during embryological development. It may be isolated or associated with visceral dextroposition or malformations.
Naif Alghasab   +13 more
doaj   +1 more source

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