Results 31 to 40 of about 2,833 (190)

Heterotaxy Polysplenia Syndrome Causing Intermittent Vomiting Due to Malrotation of the Duodenum in an Adult

open access: yesHaseki Tıp Bülteni, 2019
Heterotaxy syndrome (situs ambiguus) is a rare condition in which the internal organs are abnormally arranged in the chest and abdomen. It occurs from an early embryological developmental disturbance with most cases being sporadic.
Tuba Selçuk Can   +2 more
doaj   +1 more source

Antenatal diagnosis of left atrial isomerism and heterotaxy syndrome in fetus with Meckel-Gruber syndrome

open access: yesTürk Kardiyoloji Derneği Arşivi, 2014
We aimed to present a fetus with Meckel-Gruber syndrome (MKS) who had left atrial isomerism, heterotaxy syndrome and complete heart block. A 26-year-old healthy female was referred to our clinic in the 23rd week of her pregnancy.
Seçil Kurtulmuş   +4 more
doaj   +1 more source

Heterotaxy Syndrome and Spectrum of Cardiac Involvement

open access: yesJournal of the Indian Academy of Echocardiography & Cardiovascular Imaging
Heterotaxy syndrome, a birth defect characterized by abnormal arrangement of organs, is strongly associated with complex congenital heart disease (CHD).
Munesh Tomar, Maitri Chaudhuri
doaj   +1 more source

Novel use of covered stents to treat profound cyanosis in a hepatic vein exclusion Fontan

open access: yesAnnals of Pediatric Cardiology, 2019
Fontan completion in patients with complex cardiac anatomy, and specifically heterotaxy syndrome, can present unique physiologic considerations. For example, existing venous connections may be “unmasked” after a cavopulmonary anastomosis operation.
Sarosh P Batlivala, Makram R Ebeid
doaj   +1 more source

Aortic pseudocoarctation associated with polysplenia/heterotaxy syndrome

open access: yesRevista Portuguesa de Cardiologia, 2015
Polysplenia/heterotaxy syndrome is a rare congenital disorder associated with a wide spectrum of anomalies in various organ systems. Although anomalies of the cardiovascular system are common in this syndrome, the authors report a rare case of ...
Ricardo Duarte, Humberto Morais
doaj   +1 more source

Polysplenia syndrome with complex heart disease and jejunal atresia with malrotation in neonate: A case report

open access: yesClinical Case Reports, 2020
Polysplenia is heterotaxy syndrome or bilateral left‐sidedness. We report a case of polysplenia syndrome in order to draw attention to this rare syndrome that must be excluded in an infant presenting with congenital heart disease and intestinal ...
Roya Arif Huseynova   +4 more
doaj   +1 more source

Management for Heterotaxy Syndrome With Functional Single Ventricle and Extracardiac Total Anomalous Pulmonary Venous Connection

open access: yesTokyo Women's Medical University Journal, 2023
Background: Heterotaxy syndrome associated with functional single ventricle and extracardiac total anomalous pulmonary venous connection (TAPVC) is characterized by high operative risks and has high mortality rate.
Minori Tateishi, Masaaki Koide
doaj   +1 more source

Small RNA pathways in mammalian oocytes

open access: yesFEBS Open Bio, EarlyView.
Three distinct small RNA pathways operate in mammalian oocytes: RNAi interference (RNAi), the microRNA (miRNA) pathway, and the PIWI‐associated RNA (piRNA) pathway. These pathways use small RNAs to guide sequence‐specific repression and contribute to oocyte biology by targeting genes and mobile elements or appear insignificant since different ...
Petr Svoboda, Josef Pasulka
wiley   +1 more source

Splenic Infarct with Polysplenia Syndrome

open access: yesJournal of the Belgian Society of Radiology, 2022
A rare case of spontaneous splenic infarction with polysplenia is presented. The diagnosis was made by confirmed by enhanced computed tomography (CT), which showed multiple spleens in the left abdomen and one of the spleen showing low attenuation areas ...
Qin Ling Zhu, Wenjun Zhu
doaj   +1 more source

Association Between Motor Pathway Damage and Motor Deficit in Upper and Lower Limb in People With MS

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Corticospinal tract damage is common in people with MS, but the degree of clinical symptoms varies. We hypothesize that corticospinal tract lesions are more extensive and severe in people with MS with motor impairments in both upper and lower limbs.
Mathilde Liffran   +13 more
wiley   +1 more source

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