The Experts below are selected from a list of 39 Experts worldwide ranked by ideXlab platform

Ingrid Tonhajzerova - One of the best experts on this subject based on the ideXlab platform.

  • pulmonary artery sling a novel Cardiovascular Finding in a patient with distal 18q deletion
    Progress in Pediatric Cardiology, 2019
    Co-Authors: Tomas Jurko, Alexander Jurko, Jana Krsiakova, Milan Minarik, Michal Mestanik, Ingrid Tonhajzerova
    Abstract:

    Abstract Among the rare chromosome abnormalities compatible with life, partial monosomy of chromosome 18 is a relatively frequent chromosomal aberration. The affected individuals are at relatively increased risk of having congenital cardiac defects with the pulmonary valve anomalies and atrial septal defects being the most common Findings. We report a patient with a distal 18q deletion, follow-up from birth to 15 years of age, and a novel Finding of distal 18q-–associated Cardiovascular anomaly - a pulmonary artery sling. Since birth, the patient presented with characteristic phenotype features, respiratory distress, and frequent respiratory infections. Echocardiographic examination revealed atrial septal defect and a suspicion for presence of pulmonary artery sling, which was later confirmed using computed tomography angiocardiography. During the surgery at 18 months of age, patent ductus arteriosus was found and repaired together with repair of atrial septal defect and pulmonary artery sling. Postoperatively, the stridor and respiratory distress gradually disappeared. Since exact echocardiographic imaging of vascular anomalies can be challenging in some patients, the occurrence of pulmonary artery sling in the individuals with distal 18q deletion is likely not so exceptional, but rather it may be missed during routine echocardiographic evaluation. Therefore, the definitive diagnosis should be made using computed tomography angiocardiography, which is preferred to magnetic resonance imaging due to better visualization of lung parenchyma and airways, higher spatial resolution, and faster scanning with lower requirement of sedation. To our knowledge, this is the first report of pulmonary artery sling in a patient with a distal 18q deletion.

  • Pulmonary artery sling – A novel Cardiovascular Finding in a patient with distal 18q deletion
    Progress in Pediatric Cardiology, 2019
    Co-Authors: Tomas Jurko, Alexander Jurko, Jana Krsiakova, Milan Minarik, Michal Mestanik, Ingrid Tonhajzerova
    Abstract:

    Abstract Among the rare chromosome abnormalities compatible with life, partial monosomy of chromosome 18 is a relatively frequent chromosomal aberration. The affected individuals are at relatively increased risk of having congenital cardiac defects with the pulmonary valve anomalies and atrial septal defects being the most common Findings. We report a patient with a distal 18q deletion, follow-up from birth to 15 years of age, and a novel Finding of distal 18q-–associated Cardiovascular anomaly - a pulmonary artery sling. Since birth, the patient presented with characteristic phenotype features, respiratory distress, and frequent respiratory infections. Echocardiographic examination revealed atrial septal defect and a suspicion for presence of pulmonary artery sling, which was later confirmed using computed tomography angiocardiography. During the surgery at 18 months of age, patent ductus arteriosus was found and repaired together with repair of atrial septal defect and pulmonary artery sling. Postoperatively, the stridor and respiratory distress gradually disappeared. Since exact echocardiographic imaging of vascular anomalies can be challenging in some patients, the occurrence of pulmonary artery sling in the individuals with distal 18q deletion is likely not so exceptional, but rather it may be missed during routine echocardiographic evaluation. Therefore, the definitive diagnosis should be made using computed tomography angiocardiography, which is preferred to magnetic resonance imaging due to better visualization of lung parenchyma and airways, higher spatial resolution, and faster scanning with lower requirement of sedation. To our knowledge, this is the first report of pulmonary artery sling in a patient with a distal 18q deletion.

Tomas Jurko - One of the best experts on this subject based on the ideXlab platform.

  • pulmonary artery sling a novel Cardiovascular Finding in a patient with distal 18q deletion
    Progress in Pediatric Cardiology, 2019
    Co-Authors: Tomas Jurko, Alexander Jurko, Jana Krsiakova, Milan Minarik, Michal Mestanik, Ingrid Tonhajzerova
    Abstract:

    Abstract Among the rare chromosome abnormalities compatible with life, partial monosomy of chromosome 18 is a relatively frequent chromosomal aberration. The affected individuals are at relatively increased risk of having congenital cardiac defects with the pulmonary valve anomalies and atrial septal defects being the most common Findings. We report a patient with a distal 18q deletion, follow-up from birth to 15 years of age, and a novel Finding of distal 18q-–associated Cardiovascular anomaly - a pulmonary artery sling. Since birth, the patient presented with characteristic phenotype features, respiratory distress, and frequent respiratory infections. Echocardiographic examination revealed atrial septal defect and a suspicion for presence of pulmonary artery sling, which was later confirmed using computed tomography angiocardiography. During the surgery at 18 months of age, patent ductus arteriosus was found and repaired together with repair of atrial septal defect and pulmonary artery sling. Postoperatively, the stridor and respiratory distress gradually disappeared. Since exact echocardiographic imaging of vascular anomalies can be challenging in some patients, the occurrence of pulmonary artery sling in the individuals with distal 18q deletion is likely not so exceptional, but rather it may be missed during routine echocardiographic evaluation. Therefore, the definitive diagnosis should be made using computed tomography angiocardiography, which is preferred to magnetic resonance imaging due to better visualization of lung parenchyma and airways, higher spatial resolution, and faster scanning with lower requirement of sedation. To our knowledge, this is the first report of pulmonary artery sling in a patient with a distal 18q deletion.

  • Pulmonary artery sling – A novel Cardiovascular Finding in a patient with distal 18q deletion
    Progress in Pediatric Cardiology, 2019
    Co-Authors: Tomas Jurko, Alexander Jurko, Jana Krsiakova, Milan Minarik, Michal Mestanik, Ingrid Tonhajzerova
    Abstract:

    Abstract Among the rare chromosome abnormalities compatible with life, partial monosomy of chromosome 18 is a relatively frequent chromosomal aberration. The affected individuals are at relatively increased risk of having congenital cardiac defects with the pulmonary valve anomalies and atrial septal defects being the most common Findings. We report a patient with a distal 18q deletion, follow-up from birth to 15 years of age, and a novel Finding of distal 18q-–associated Cardiovascular anomaly - a pulmonary artery sling. Since birth, the patient presented with characteristic phenotype features, respiratory distress, and frequent respiratory infections. Echocardiographic examination revealed atrial septal defect and a suspicion for presence of pulmonary artery sling, which was later confirmed using computed tomography angiocardiography. During the surgery at 18 months of age, patent ductus arteriosus was found and repaired together with repair of atrial septal defect and pulmonary artery sling. Postoperatively, the stridor and respiratory distress gradually disappeared. Since exact echocardiographic imaging of vascular anomalies can be challenging in some patients, the occurrence of pulmonary artery sling in the individuals with distal 18q deletion is likely not so exceptional, but rather it may be missed during routine echocardiographic evaluation. Therefore, the definitive diagnosis should be made using computed tomography angiocardiography, which is preferred to magnetic resonance imaging due to better visualization of lung parenchyma and airways, higher spatial resolution, and faster scanning with lower requirement of sedation. To our knowledge, this is the first report of pulmonary artery sling in a patient with a distal 18q deletion.

Jeremy Rogers - One of the best experts on this subject based on the ideXlab platform.

  • AIME - Interface of Inference Models with Concept and Medical Record Models
    Artificial Intelligence in Medicine, 2001
    Co-Authors: Alan L. Rector, Peter D. Johnson, Chris Wroe, Jeremy Rogers
    Abstract:

    Medical information systems and standards are increasingly based on principled models of at least three distinct sorts of information - patient data, concepts (terminology), and guidelines (decision support). Well defined interfaces are required between the three types of model to allow development to proceed independently. Two of the major issues to be dealt with in the defining of such interfaces are the interaction between ontological and inferential abstractions - how general notions such as 'abnormal Cardiovascular Finding' are abstracted from concrete data - and the management of the meaning of information in guidelines in different contexts. This paper explores these two issues and their ramifications.

Alexander Jurko - One of the best experts on this subject based on the ideXlab platform.

  • pulmonary artery sling a novel Cardiovascular Finding in a patient with distal 18q deletion
    Progress in Pediatric Cardiology, 2019
    Co-Authors: Tomas Jurko, Alexander Jurko, Jana Krsiakova, Milan Minarik, Michal Mestanik, Ingrid Tonhajzerova
    Abstract:

    Abstract Among the rare chromosome abnormalities compatible with life, partial monosomy of chromosome 18 is a relatively frequent chromosomal aberration. The affected individuals are at relatively increased risk of having congenital cardiac defects with the pulmonary valve anomalies and atrial septal defects being the most common Findings. We report a patient with a distal 18q deletion, follow-up from birth to 15 years of age, and a novel Finding of distal 18q-–associated Cardiovascular anomaly - a pulmonary artery sling. Since birth, the patient presented with characteristic phenotype features, respiratory distress, and frequent respiratory infections. Echocardiographic examination revealed atrial septal defect and a suspicion for presence of pulmonary artery sling, which was later confirmed using computed tomography angiocardiography. During the surgery at 18 months of age, patent ductus arteriosus was found and repaired together with repair of atrial septal defect and pulmonary artery sling. Postoperatively, the stridor and respiratory distress gradually disappeared. Since exact echocardiographic imaging of vascular anomalies can be challenging in some patients, the occurrence of pulmonary artery sling in the individuals with distal 18q deletion is likely not so exceptional, but rather it may be missed during routine echocardiographic evaluation. Therefore, the definitive diagnosis should be made using computed tomography angiocardiography, which is preferred to magnetic resonance imaging due to better visualization of lung parenchyma and airways, higher spatial resolution, and faster scanning with lower requirement of sedation. To our knowledge, this is the first report of pulmonary artery sling in a patient with a distal 18q deletion.

  • Pulmonary artery sling – A novel Cardiovascular Finding in a patient with distal 18q deletion
    Progress in Pediatric Cardiology, 2019
    Co-Authors: Tomas Jurko, Alexander Jurko, Jana Krsiakova, Milan Minarik, Michal Mestanik, Ingrid Tonhajzerova
    Abstract:

    Abstract Among the rare chromosome abnormalities compatible with life, partial monosomy of chromosome 18 is a relatively frequent chromosomal aberration. The affected individuals are at relatively increased risk of having congenital cardiac defects with the pulmonary valve anomalies and atrial septal defects being the most common Findings. We report a patient with a distal 18q deletion, follow-up from birth to 15 years of age, and a novel Finding of distal 18q-–associated Cardiovascular anomaly - a pulmonary artery sling. Since birth, the patient presented with characteristic phenotype features, respiratory distress, and frequent respiratory infections. Echocardiographic examination revealed atrial septal defect and a suspicion for presence of pulmonary artery sling, which was later confirmed using computed tomography angiocardiography. During the surgery at 18 months of age, patent ductus arteriosus was found and repaired together with repair of atrial septal defect and pulmonary artery sling. Postoperatively, the stridor and respiratory distress gradually disappeared. Since exact echocardiographic imaging of vascular anomalies can be challenging in some patients, the occurrence of pulmonary artery sling in the individuals with distal 18q deletion is likely not so exceptional, but rather it may be missed during routine echocardiographic evaluation. Therefore, the definitive diagnosis should be made using computed tomography angiocardiography, which is preferred to magnetic resonance imaging due to better visualization of lung parenchyma and airways, higher spatial resolution, and faster scanning with lower requirement of sedation. To our knowledge, this is the first report of pulmonary artery sling in a patient with a distal 18q deletion.

Jana Krsiakova - One of the best experts on this subject based on the ideXlab platform.

  • pulmonary artery sling a novel Cardiovascular Finding in a patient with distal 18q deletion
    Progress in Pediatric Cardiology, 2019
    Co-Authors: Tomas Jurko, Alexander Jurko, Jana Krsiakova, Milan Minarik, Michal Mestanik, Ingrid Tonhajzerova
    Abstract:

    Abstract Among the rare chromosome abnormalities compatible with life, partial monosomy of chromosome 18 is a relatively frequent chromosomal aberration. The affected individuals are at relatively increased risk of having congenital cardiac defects with the pulmonary valve anomalies and atrial septal defects being the most common Findings. We report a patient with a distal 18q deletion, follow-up from birth to 15 years of age, and a novel Finding of distal 18q-–associated Cardiovascular anomaly - a pulmonary artery sling. Since birth, the patient presented with characteristic phenotype features, respiratory distress, and frequent respiratory infections. Echocardiographic examination revealed atrial septal defect and a suspicion for presence of pulmonary artery sling, which was later confirmed using computed tomography angiocardiography. During the surgery at 18 months of age, patent ductus arteriosus was found and repaired together with repair of atrial septal defect and pulmonary artery sling. Postoperatively, the stridor and respiratory distress gradually disappeared. Since exact echocardiographic imaging of vascular anomalies can be challenging in some patients, the occurrence of pulmonary artery sling in the individuals with distal 18q deletion is likely not so exceptional, but rather it may be missed during routine echocardiographic evaluation. Therefore, the definitive diagnosis should be made using computed tomography angiocardiography, which is preferred to magnetic resonance imaging due to better visualization of lung parenchyma and airways, higher spatial resolution, and faster scanning with lower requirement of sedation. To our knowledge, this is the first report of pulmonary artery sling in a patient with a distal 18q deletion.

  • Pulmonary artery sling – A novel Cardiovascular Finding in a patient with distal 18q deletion
    Progress in Pediatric Cardiology, 2019
    Co-Authors: Tomas Jurko, Alexander Jurko, Jana Krsiakova, Milan Minarik, Michal Mestanik, Ingrid Tonhajzerova
    Abstract:

    Abstract Among the rare chromosome abnormalities compatible with life, partial monosomy of chromosome 18 is a relatively frequent chromosomal aberration. The affected individuals are at relatively increased risk of having congenital cardiac defects with the pulmonary valve anomalies and atrial septal defects being the most common Findings. We report a patient with a distal 18q deletion, follow-up from birth to 15 years of age, and a novel Finding of distal 18q-–associated Cardiovascular anomaly - a pulmonary artery sling. Since birth, the patient presented with characteristic phenotype features, respiratory distress, and frequent respiratory infections. Echocardiographic examination revealed atrial septal defect and a suspicion for presence of pulmonary artery sling, which was later confirmed using computed tomography angiocardiography. During the surgery at 18 months of age, patent ductus arteriosus was found and repaired together with repair of atrial septal defect and pulmonary artery sling. Postoperatively, the stridor and respiratory distress gradually disappeared. Since exact echocardiographic imaging of vascular anomalies can be challenging in some patients, the occurrence of pulmonary artery sling in the individuals with distal 18q deletion is likely not so exceptional, but rather it may be missed during routine echocardiographic evaluation. Therefore, the definitive diagnosis should be made using computed tomography angiocardiography, which is preferred to magnetic resonance imaging due to better visualization of lung parenchyma and airways, higher spatial resolution, and faster scanning with lower requirement of sedation. To our knowledge, this is the first report of pulmonary artery sling in a patient with a distal 18q deletion.