Results 81 to 90 of about 1,222,131 (133)

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

CHRONIC ATRIAL FIBRILLATION IN PRESENCE OF AORTIC STENOSIS IN A PATIENT WITH POLYSPLENIA SYNDROME

open access: yes, 2013
We report a rare case of "situs viscerum ambiguous" with polysplenia syndrome, in a 69 year old female patient with aortic stenosis and chronic atrial fibrillation.
Trovato, RL   +6 more
core   +1 more source

A Rare Variation of the Heterotaxy Syndrome

open access: yesCase Reports in Medicine, 2012
Heterotaxy syndrome is a rare, complex, and confusing type of the situs anomalies. It is not possible to estimate the degree of lateralization, isomerism, and rotational variation in these types of cases.
Alper Dilli   +4 more
doaj   +1 more source

Echocardiography in Heterotaxy Syndrome

open access: yes, 2011
The important anatomic aspects of heterotaxy syndrome can be diagnosed by Doppler echocardiography in the newborn and infant. An organized approach and an understanding of asplenia (right atrial isomerism) and polysplenia (left atrial isomerism) are ...
Gerald R. Marx
core   +1 more source

Polysplenia Syndrome Complicated by Splenic Infarction: A Report of a Rare Case. [PDF]

open access: yesCureus, 2023
Abdullah RA   +5 more
europepmc   +1 more source

Heterotaxy syndrome with agenesis of dorsal pancreas and diabetes mellitus: case report and review of the literature

open access: yesArchives of Endocrinology and Metabolism
SUMMARY Heterotaxy syndrome (HS) is a rare congenital condition with multifactorial heritance, characterized by an abnormal arrangement of thoraco-abdominal organs and vessels.
Cínthia Minatel Riguetto   +2 more
doaj   +1 more source

Syndromic variants of biliary atresia

open access: yesWorld Journal of Pediatric Surgery
Biliary atresia (BA) may be characterized as an obliterative cholangiopathy presenting in the newborn period with conjugated jaundice, pale stools, and dark urine. It is usually thought of as an isolated anomaly in otherwise normal infants. However, in a
Mark Davenport
doaj   +1 more source

Polysplenia syndrome revealed in adulthood by pancreatic and vascular malformations: a case report. [PDF]

open access: yesPan Afr Med J, 2022
Mountassir ME   +5 more
europepmc   +1 more source

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