Results 31 to 40 of about 9,312 (200)

Outcome of prenatally diagnosed fetal heterotaxy: A systematic review and meta-analysis. [PDF]

, 2017
OBJECTIVES: To assess the perinatal outcomes of fetuses affected by heterotaxy. METHODS: Medline, Embase and Cinhal were searched. Only studies reporting a prenatal diagnosis of isomerism were included.
Abuhamad, Atkinson, Bardin, Baschat, Berg, Bronshtein, Brueckner, Carvalho, Collins, Degenhardt, Ditchfield, Dreux, Egger, Escobar-Diaz, Friedberg, Gaur, Gottschalk, Henderson, Ho, Hoefstaetter, Hunter, Icardo, Jacobs, Kennedy, Kheiri, Kothari, Ladd, Lee, Leeflang, Lim, Lin, Loomba, Loomba, Manzoli, McKiernan, Nakada, Nemec, NHS Centre for Reviews and Dissemination, Ozkutlu, Paladini, Pasquini, Peoples, Pepes, Phoon, Pockett, Shen, Shen, Taketazu, Tan, Tan, Varela-Fascinetto, Yan   +51 more
core   +1 more source

Streptococcus pneumoniae Infection in Patients with Asplenia: A Spanish Perspective over a 25-Year Period

Antibiotics
Anatomical or functional asplenia constitutes a risk factor for Streptococcus pneumoniae (SP) infection, being more frequent in children and the elderly and in people with multiple comorbidities.
Enrique Gea-Izquierdo, Gil Rodríguez-Caravaca, Ruth Gil-Prieto, Valentín Hernández-Barrera, Ángel Gil-de-Miguel   +4 more
doaj   +1 more source

Ultrastructural and morphometric analysis of enlarged platelets in congenital isolated asplenia [PDF]

Vojnosanitetski Pregled, 2019
Introduction. Congenital asplenia is an extremely rare condition that can be separate entity due to a specific defect of spleen development or may occur in the context of a malformation syndrome.
Marković Olivera, Martinović Tamara, Ćirić Darko, Trpinac Dušan, Čemerikić-Martinović Vesna, Bumbaširević Vladimir, Bila Jelena, Marisavljević Dragomir, Kravić-Stevović Tamara   +8 more
doaj   +1 more source

Germline 3p22.1 microdeletion encompassing RPSA gene is an ultra-rare cause of isolated asplenia

Molecular Cytogenetics, 2021
Background Isolated Congenital Asplenia (ICA, OMIM #271400) is a rare, life-threatening abnormality causing immunodeficiency, which is characterized by the absence of a spleen.
Aleksandra Oszer, Katarzyna Bąbol-Pokora, Sylwia Kołtan, Agata Pastorczak, Wojciech Młynarski   +4 more
doaj   +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

Elixhauser comorbidity method in predicting death of Spanish inpatients with asplenia and pneumococcal pneumonia

BMC Infectious Diseases
Background Pneumococcal pneumonia (PP) is a serious infection caused by Streptococcus pneumoniae (pneumococcus), with a wide spectrum of clinical manifestations.
Enrique Gea-Izquierdo, Rossana Ruiz-Urbaez, Valentín Hernández-Barrera, Michael Stich, Ángel Gil-de-Miguel   +4 more
doaj   +1 more source

Early and long-term outcomes following cardiac surgery for patients with heterotaxy syndromeCentral MessagePerspective

JTCVS Open
Objective: Heterotaxy syndrome is a complex multisystem abnormality historically associated with high morbidity and mortality. We sought to evaluate the early and long-term outcomes after cardiac surgery in heterotaxy syndrome.
Victor S. Alemany, MD, MS, Alexis Crawford, BA, Kimberlee Gauvreau, ScD, Emily M. Bucholz, MD-PhD, MPH, Pedro J. del Nido, MD, David N. Schidlow, MD, MMus, Meena Nathan, MD, MPH   +6 more
doaj   +1 more source

Pulmonary Hemodynamic Changes with Nitric Oxide or Oxygen in a Patient with Asplenia, Single Right Ventricle, and Total Anomalous Pulmonary Venous Connection after Fontan Procedure

Case Reports in Cardiology, 2018
Asplenia syndrome is frequently complicated by a total anomalous pulmonary venous connection. Pulmonary venous obstruction, following total anomalous pulmonary venous connection surgery, is one of the risk factors for morbidity and mortality.
Hideharu Oka, Kouichi Nakau, Aya Kajihama, Masaya Sugimoto, Hiroshi Azuma   +4 more
doaj   +1 more source

Yield of Whole Genome Sequencing for Pathogenic Single Nucleotide Variants in Congenital Heart Disease: A Systematic Review and Meta‐Analysis

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective This systematic review and meta‐analysis aimed to assess the diagnostic yield of pathogenic or likely pathogenic (P/LP) single nucleotide variants (SNVs) using whole genome sequencing (WGS) in congenital heart disease (CHD). Methods A systematic search of three databases (2000–2024) was conducted, and two reviewers independently ...
Hiba J. Mustafa, Parisa Najjariasl, Faezeh Aghajani, Enaja V. Sambatur, Andrew Rodenbarger, Stephanie Guseh, Amy E. Roberts, Alireza A. Shamshirsaz   +7 more
wiley   +1 more source

Vacunación en neumococo. Actuación en la farmacia comunitaria [PDF]

, 2016
En la elaboración del documento han participado SEFAC, semFYC, SEMERGEN y SEPAR. El objetivo principal era definir los perfiles de paciente susceptibles prioritariamente de la vacunación frente al neumococo considerando los grupos de riesgo, las ...
Casas Jansá, Ricard, Molina París, Jesús, Quintano Jiménez, José Antonio, Rodríguez González-Moro, José Miguel   +3 more
core   +1 more source