Results 31 to 40 of about 2,012 (189)

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

Agenesis of the Dorsal Pancreas: Case Report and Review of Age‐Related Differences in Presentation

open access: yesJPGN Reports, Volume 4, Issue 3, August 2023., 2023
Agenesis of the dorsal pancreas (ADP) is a rare congenital anomaly that occurs when the body and tail of the pancreas fail to develop from the dorsal bud in utero. ADP may be discovered when evaluating conditions arising from the anomaly, such as diabetes mellitus, pancreatitis, and pancreatic insufficiency, but is more commonly found as an incidental ...
Callie A. Grey   +3 more
wiley   +1 more source

Polysplenia syndrome with situs ambiguous, common mesentery, and IVC interruption discovered incidentally in an adult

open access: yesRadiology Case Reports, 2019
Polysplenia syndrome associates multiple spleens to other malformations, most frequently cardiac, vascular, visceral, and biliary malformations. Polysplenia has been described mainly in childhood owing to critical anatomic malformations related to ...
Hajar El Mortaji   +3 more
doaj   +1 more source

Clinical heterogeneity of NADSYN1‐associated VCRL syndrome

open access: yesClinical Genetics, Volume 104, Issue 1, Page 114-120, July 2023., 2023
Clinicians should suspect NAD deficiency disorder when a patient presents with congenital malformations, especially when vertebral, cardiac, renal, or limb defects are present. We expanded NAD deficiency disorder spectrum with the presentation of three cases from two unrelated families, with high inter‐ and intra‐familial variability.
Marion Aubert‐Mucca   +10 more
wiley   +1 more source

Polysplenia and other anatomical variants of the spleen

open access: yesJournal of Education, Health and Sport, 2022
The anatomy, physiology and embryology of the spleen are essential fields of study for the determination of congenital varieties as well as the pathological processes occurring in this organ.The aim of this study is to summarize the current knowledge on
Agnieszka Kopystecka   +5 more
doaj   +1 more source

Heterotaxy pattern associated with sinus node dysfunction in an adult: A case report

open access: yesClinical Case Reports, 2023
Key Clinical Message A 26‐year‐old male patient admitted to the hospital ward with experience of repetitive syncopes for a year. The patient was diagnosed with sick sinus syndrome.
Naman Shah   +8 more
doaj   +1 more source

Risk factors for Fontan-associated hepatocellular carcinoma.

open access: yesPLoS ONE, 2022
AimsThe incidence of hepatocellular carcinoma (HCC) in patients with Fontan-associated liver disease (i.e., FALD-HCC) has increased over time. However, the risk factors for HCC development remain unclear.
Tomomi Kogiso   +6 more
doaj   +1 more source

Splenic Torsion in Heterotaxy Syndrome with Left Isomerism: A Case Report and Literature Review

open access: yesDiagnostics, 2022
Splenic torsion is an unusual condition that results in congenital abnormality, especially in the visceral abnormal arrangement. We report the case of an 8.5-year-old boy with features in the right upper quadrant.
I Nok Cheang   +4 more
doaj   +1 more source

A CASE OF COR BILOCULARE ACCOMPANIED BY POLYSPLENIA [PDF]

open access: yesActa Medica Iranica, 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
doaj   +2 more sources

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