Results 61 to 70 of about 1,970 (197)

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

Clinical 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, Behnam Dalfardi, Ali Nemati, Sina Bakhshaei, Elahenaz Parsi mood   +4 more
wiley   +1 more source

Polüspleeniaga heterotaksia sündroom [PDF]

, 2015
Eesti Arst 2015; 94(11):675 ...
Tiivel, Marek
core   +2 more sources

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

Journal 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, Anne Larroque‐Devigne, Dominique Forgues, Eve Mousty, Alain Couture, Nicolas Kalfa, Olivier Prodhomme, Florent Fuchs   +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

Radiology 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

Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia [PDF]

, 2010
Generalised lymphatic dysplasia (GLD) is characterised by extensive peripheral lymphoedema with visceral involvement. In some cases, it presents in utero with hydrops fetalis. Autosomal dominant and recessive inheritance has been reported.
Brice, G, Bunyan, DJ, Connell, F, Homfray, T, Jeffery, S, Kalidas, K, Lymphoedema Consortium, Mansour, S, Mitton, S, Mortimer, P, Ostergaard, P, Roberts, L   +11 more
core   +1 more source

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

Pediatrics 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, Chiyoe Shirota, Motoshi Wada, Masato Shinkai, Hirofumi Tomita, Satoshi Umeda, Hiromu Miyake, Toshiharu Matsuura, Shigehisa Fumino, Akio Odaka, Taizo Hibi, Toshio Harumatsu, Akiko Yokoi, Tomoro Hishiki, Shigeru Ono, Kohei Matsushita, the Japanese Biliary Atresia Society   +16 more
wiley   +1 more source

Appropriate Route Selection for Extracardiac Total Cavopulmonary Connection in Apicocaval Juxtaposition [PDF]

, 2012
BACKGROUND:A malpositioned heart with apicocaval juxtaposition may complicate the management of patients with functional single ventricles when total cavopulmonary connection is performed.
Abe Masakazu, Hiramatsu Yuji, Kanemoto Shinya, Kato Hideyuki, Morizumi Sei, Noma Mio, Sakakibara Yuzuru, 平松 祐司, 榊原 謙, 金本 真也   +9 more
core   +1 more source

Left Isomerism With Normal Bronchopulmonary Anatomy: Broadening the Heterotaxy Spectrum

Case 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, Erin Moffett, Madison Wulfeck, Dennis Lindfors, Sandor Szilagyi, Atsushi Komemushi   +5 more
wiley   +1 more source

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

Journal 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, Dinesh Kumar Thapa, Dinesh Pokhrel, Amit Kumar Shah   +3 more
doaj   +1 more source

Fetal Presentation of MYRF‐Related Cardiac Urogenital Syndrome: An Emerging and Challenging Prenatal Diagnosis

Prenatal Diagnosis, Volume 44, Issue 13, Page 1647-1658, December 2024.
ABSTRACT Purpose MYRF‐related cardiac‐urogenital syndrome (MYRF‐CUGS) is a rare condition associated with heterozygous MYRF variants. The description of MYRF‐CUGS phenotype is mostly based on postnatal cases and 36 affected individuals have been published so far.
Maud Favier, Elise Brischoux‐Boucher, Louise C. Pyle, Nicolas Mottet, Marion Auber‐Lenoir, Julie Cattin, Eric Dahlen, Christelle Cabrol, Francine Arbez‐Gindre, Tania Attié‐Bitach, Odile Boute, Louise Devisme, Detlef Trost, Aicha Boughalem, David Chitayat, Lev Prasov, Odelia Chorin, Annick Rein‐Rothschild, Eran Kassif, Tal Weissbach, Laura Godfrey Hendon, Margaret P. Adam, Chloé Quelin, Sylvie Jaillard, Laura Mary, Sietse M. Aukema, Malou Heijligers, Christine de Die‐Smulders, Sander Stegmann, Lauren Badalato, Adi Ben‐Yehuda, Claire Beneteau, Pierre‐Louis Forey, Paul Kuentz, Juliette Piard   +34 more
wiley   +1 more source