Results 91 to 100 of about 1,222,131 (133)
Polysplenia syndrome in adulthood: a case report. [PDF]
Pan Afr Med J, 2022 Malki MC +9 more
europepmc +1 more source
Urology Case ReportsZinner syndrome is a congenital anomaly characterized by seminal vesicle cysts, ipsilateral renal agenesis, and ejaculatory duct obstruction possibly associated with infertility. Only 200 cases of Zinner syndrome have been reported since its discovery in
Tzu-Yu Chiu +4 more
doaj +1 more source
Laparoscopic splenectomy for polysplenia with splenic torsion: a case report
, 2019 Background Polysplenia refers to the presence of two or more equal-sized spleens. Very rarely, one of the multiple spleens may develop torsion and infarction.
Tomoyuki Nagata +7 more
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A CASE OF COR BILOCULARE ACCOMPANIED BY POLYSPLENIA [PDF]
, 1972 The clinical history and necroscopic fi ndings of a 3 -} year old girl - involved in cor biloculare was reported. In th is case dextrotransposition of the great a rteries and polysplenia was observed. The majority of cor biloculare cases appearing in the
M. S. ROJHAN
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Long-term survival and phenotypic spectrum in heterotaxy syndrome: a 25-year follow-up experience
, 2018 Background: Heterotaxy syndrome (HS) is a group of congenital disorders characterized by abnormal arrangement of thoraco-abdominal organs across the left-right axis of the body, classified as right (RAI) and left atrial isomerism (LAI)·We investigated ...
Baban, Anwar +13 more
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Esophageal duplication cyst coexisting with Bochdalek's hernia and polysplenia
, 1999 Esophageal duplication cyst, Bochdalek's hernia and polysplenia are uncommon congenital anomalies which have not been reported to be associated with each other.
Igci, E +4 more
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Splenic Duplication, a Rare Cause of Gastric Varices: A Case Report
Journal of the Korean Society of RadiologySplenic duplication, also known as polysplenia syndrome, is a condition occasionally observed in which the spleen is divided into segments of similar size.
Seul Ki Kim, Tae Young Lee
doaj +1 more source
An Unusual Case of Heterotaxy Syndrome [PDF]
Introduction: Heterotaxy syndrome (HS), also referred to as situs ambiguous, is a rare congenital condition marked by the abnormal positioning and asymmetry of thoracoabdominal organs in relation to the body\u27s midline.
Kosoy, David +4 more
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