Results 61 to 70 of about 1,957 (209)

Heterotaxy Syndrome In A Middle-Aged Pakistani Male [PDF]

open access: yes, 2023
Background: Heterotaxy syndrome (or situs ambiguous) is an extremely rare disorder in which the viscera are arranged in an abnormally asymmetrical pattern around the midline along with cardiac and spleen abnormalities.
Din, Ahsan Tameez ud   +4 more
core   +2 more sources

De novo deletions and duplications of 17q25.3 cause susceptibility to cardiovascular malformations [PDF]

open access: yes, 2015
BACKGROUND: Genomic disorders resulting from deletion or duplication of genomic segments are known to be an important cause of cardiovascular malformations (CVMs).
Austin, E.   +18 more
core   +1 more source

Massive Hemoptysis in a Patient With Eisenmenger Syndrome, Polysplenia and Transverse Liver

open access: yesClinical Case Reports, Volume 13, Issue 3, March 2025.
ABSTRACT Hemoptysis is defined as blood‐streaked sputum from the lower parts of the respiratory tract. Hemoptysis, even in small amounts, is a frightening and alarm sign for possible underlying conditions such as infections, pulmonary diseases, neoplastic conditions, cardiovascular alterations, vasculitis, traumatic events, hematological derangements ...
Mohsen Shafiepour   +4 more
wiley   +1 more source

Performance of Prenatal Ultrasound Screening for the Relative Positioning of Mesenteric Vessels

open access: yesJournal of Ultrasound in Medicine, Volume 44, Issue 1, Page 35-45, January 2025.
Objectives Abnormal relative positioning of the superior mesenteric artery (SMA) and vein (SMV) can lead to intestinal malrotation that predisposes to midgut volvulus. The aim of this study was to assess the prenatal ultrasound ability to visualize the relative position of SMA and SMV in normal pregnancies. Methods Prospective cohort study performed in
Jean Michel Faure   +7 more
wiley   +1 more source

Polysplenia with situs inversus totalis, azygos continuation of the inferior vena cava, and duplication of the superior vena cava in a healthy adult: A case report

open access: yesRadiology Case Reports
Polysplenia syndrome is an embryological disorder whereby the usual left-right asymmetry of thoracic and abdominal viscera fails to develop. It is a rare entity, estimated to occur at a frequency of 1 in 40,000, and is often associated with cardiac and ...
Rahman Ladak, HBSc, William Magnuson, MD
doaj   +1 more source

Vitamin K deficiency bleeding and optimal prophylaxis methods in biliary atresia: A surveillance study in Japan

open access: yesPediatrics International, Volume 67, Issue 1, January/December 2025.
Abstract Background Vitamin K (VK) prophylaxis refers to the administration of VK to newborns to prevent neonatal VK deficiency bleeding (VKDB), which is characterized by intracranial hemorrhage (ICH). This study investigated the relationship between VK prophylaxis methods and VKDB in biliary atresia (BA).
Ryuji Okubo   +16 more
wiley   +1 more source

Syndrome! Polysplenia ina 10 year old girl [PDF]

open access: yes, 2014
We present a case of 10 year old patient with polysplenia, situs inversus abdominus, malrotation of bowel and renal anomalies. Polyspenia Syndrome refers to presence of two or more spleens associated with various abnormalities in chest and abdomen. Situs
El Awad, Mahmoud   +3 more
core   +2 more sources

Left Isomerism With Normal Bronchopulmonary Anatomy: Broadening the Heterotaxy Spectrum

open access: yesCase Reports in Radiology, Volume 2025, Issue 1, 2025.
Situs ambiguous is a rare congenital condition characterized by the abnormal arrangement of thoracoabdominal organs along the left–right axis. This condition often presents as either left or right isomerism, leading to complex anatomical variations and associated clinical challenges.
Zach Sukin   +5 more
wiley   +1 more source

Persistent Mullerian Duct Syndrome with Polysplenia and Short Pancreas: A Case Report

open access: yesJournal of Nepal Medical Association, 2019
Persistent Mullerian duct syndrome is a rare entity and usually presents with common symptoms of undescended testis and hernia. The syndrome is caused by an insufficient amount of Mullerian inhibiting substance or due to the insensitivity of the target ...
Umesh Kumar Sharma   +3 more
doaj   +1 more source

CHD associated with syndromic diagnoses: peri-operative risk factors and early outcomes [PDF]

open access: yes, 2015
CHD is frequently associated with a genetic syndrome. These syndromes often present specific cardiovascular and non-cardiovascular co-morbidities that confer significant peri-operative risks affecting multiple organ systems.
Cooper, David S.   +2 more
core   +1 more source

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