Results 101 to 110 of about 1,970 (197)

Recommendations for cardiovascular magnetic resonance in adults with congenital heart disease from the respective working groups of the European Society of Cardiology [PDF]

, 2017
This paper aims to provide information and explanations regarding the clinically relevant options, strengths, and limitations of cardiovascular magnetic resonance (CMR) in relation to adults with congenital heart disease (CHD).
Geva, Tal, Kaemmerer, Harald, Kilner, Philip J., Schwitter, Juerg, Trindade, Pedro T., Webb, Gary D.   +5 more
core  

Polysplenia syndrome

Journal of Visceral Surgery, 2011
B, De La Villeon, S, Le Goudeveze, Y, Goudard, M, Fondin, A, Vauchaussade De Chaumont, V, Duverger   +5 more
openaire   +2 more sources

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

Archives 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, Samantha Pelichek, Arnaldo Moura Neto   +2 more
doaj   +1 more source

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

Pan Afr Med J, 2022
Mountassir ME, Borahma M, Benelbarhdadi I, Lagdali N, Hosni A, Ajana FZ.   +5 more
europepmc   +1 more source

Preliminary experience with cardiovascular magnetic resonance in evaluation of fetal cardiovascular anomalies [PDF]

, 2013

core   +1 more source

Syndromic variants of biliary atresia

World 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

Zinner syndrome incidentally diagnosed in a man with ureteropelvic junction stone and hydronephrosis: A case report

Urology Case Reports
Zinner 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, Szu-Ju Chen, Chun-Lin Huang, Chi-Ping Huang, Wen-Chi Chen   +4 more
doaj   +1 more source

Double primary malignancies associated with colon cancer in patients with situs inversus totalis: two case reports [PDF]

, 2011
Young Wan Kim, Hoon Ryu, Dae Sung Kim, Ik Yong Kim, Kim, Young Wan   +4 more
core   +1 more source

Situs inversus abdominalis and duodenal atresia. A case report and review of the literature [PDF]

, 2009
Fewer than 20 patients born with situs inversus and duodenal atresia have been reported in the literature. We present a patient with this condition. A newborn baby presented shortly after birth with persistent bilious vomiting.
Brown, Craig, Numanoglu, A L P, Rode, Heinz, Sidler, Daniel   +3 more
core   +1 more source

Laparoscopic sleeve gastrectomy in polysplenia syndrome/left isomerism: A case report. [PDF]

Int J Surg Case Rep, 2020
Jeragh F, Aljazzaf I, Al Khayyat H.
europepmc   +1 more source