Results 81 to 90 of about 1,222,131 (133)
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
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
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
The Successful Management of Gangrenous Pneumococcal Infection in an Infant With Polysplenia Syndrome. [PDF]
Garout W.
europepmc +1 more source
Echocardiography in Heterotaxy Syndrome
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]
Abdullah RA +5 more
europepmc +1 more source
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
Splenic Infarct with Polysplenia Syndrome. [PDF]
Zhu QL, Zhu W.
europepmc +1 more source
Syndromic variants of biliary atresia
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]
Mountassir ME +5 more
europepmc +1 more source

