P01.16: Prenatal diagnosis of ventricular aneurysm: clinical management and outcome

2004 ◽  
Vol 24 (3) ◽  
pp. 273-273
Author(s):  
L. Pasquini ◽  
R. Wimalasundera ◽  
Y. S. Ho ◽  
M. Sheppard ◽  
H. Gardiner
Keyword(s):  
Prenatal Diagnosis ◽  
Clinical Management ◽  
Ventricular Aneurysm

scholarly journals P02.49: Prenatal diagnosis and clinical management of the body stalk anomaly during gestation. The importance of the precocious diagnostic

2006 ◽  
Vol 28 (4) ◽  
pp. 534-534
Author(s):  
E. Cordioli ◽  
L. C. S. Bussamra ◽  
G. Lobo ◽  
C. A. Souza ◽  
W. J. Hisaba ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Clinical Management ◽  
The Body

scholarly journals Umbilical Cord Hematoma: A Case Report and Review of the Literature

2018 ◽  
Vol 2018 ◽  
pp. 1-6 ◽  
Author(s):  
Gennaro Scutiero ◽  
Bernardi Giulia ◽  
Piergiorgio Iannone ◽  
Luigi Nappi ◽  
Danila Morano ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Umbilical Cord ◽  
Clinical Management ◽  
Case Reports ◽  
Rare Complication ◽  
Pregnancy Complication ◽  
Predisposing Factors ◽  
Potential Outcomes ◽  
Review Of The Literature ◽  
Exact Etiology

Objectives. To deepen the knowledge in obstetrics on a very rare pregnancy complication: umbilical cord hematoma. Methods. A review of the case reports described in the last ten years in the literature was conducted in order to evaluate epidemiology, predisposing factors, potential outcomes, prenatal diagnosis, and clinical management. Results. Spontaneous umbilical cord hematoma is a rare complication of pregnancy which represents a serious cause of fetal morbidity and mortality. There are many risk factors such as morphologic anomalies, infections, vessel wall abnormalities, iatrogenic causes, and traction or torsion of the cord, but the exact etiology is still unknown. Conclusions. Due to the rarity of this condition, every new case of umbilical cord hematoma should be reported in order to improve the knowledge of predisposing factors, prenatal diagnosis, and clinical management.

scholarly journals Clinical management of pregnancies with positive screening results for rare autosomal aneuploidies at a single center

2020 ◽  
Vol 48 (11) ◽  
pp. 030006052096687
Author(s):  
Lingshan Gou ◽  
Yuan Fang ◽  
Na Wang ◽  
Man Zhang ◽  
Tianya Liu ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Pregnancy Outcomes ◽  
Clinical Management ◽  
Uniparental Disomy ◽  
Prenatal Testing ◽  
Normal Pregnancy ◽  
Chromosomal Microarray ◽  
Chromosomal Microarray Analysis ◽  
Single Center ◽  
Trisomy 7

Objective To review our experiences on clinical management of pregnancies with positive noninvasive prenatal testing (NIPT) results for rare autosomal aneuploidies (RAAs) at a single center. Methods We performed a retrospective study and reviewed data from 18,016 pregnancies undergoing NIPT at a single center in China from March 2017 to February 2020. Depending on the patient’s choice, women with positive screening results for RAAs underwent chromosomal microarray analysis for invasive prenatal diagnosis. Results Thirty-three positive cases for RAAs were identified, with a positive screening rate of 0.18%. The most common RAA was trisomy 7 (33.3%), while trisomies for other chromosomes were less frequent. Monosomies involving chromosomes 16, 14, and 22 were observed. Twenty-eight cases of RAAs underwent invasive diagnosis. Abnormal pregnancy outcomes were observed in four cases, including true fetal mosaicism (n=1), partial uniparental disomy (n=1), miscarriage (n=1), and structural anomalies on ultrasound (n=1). Conclusions RAAs at NIPT might be associated with fetal uniparental disomy, mosaic aneuploidy, and poor pregnancy outcomes, but most positive cases have normal pregnancy outcomes. For RAAs, genetic counseling on the potential risks of abnormal NIPT results, as well as on benefits and limitations of invasive prenatal diagnosis, might help guide clinical management.

Prenatal diagnosis of ventricular aneurysm: a report of two cases and a review

2002 ◽  
Vol 22 (2) ◽  
pp. 131-136 ◽  
Author(s):  
Salvatore Pipitone ◽  
Velio Sperandeo ◽  
Maurizio Mongiovi ◽  
Grillo Roberto ◽  
Giuseppe Centineo
Keyword(s):  
Prenatal Diagnosis ◽  
Ventricular Aneurysm

scholarly journals Two Cases of Leigh Syndrome in One Family: Diagnostic Challenges and Clinical Management Experience in Latvia

2021 ◽  
Vol 2021 ◽  
pp. 1-5
Author(s):  
Arta Katkevica ◽  
Madara Kreile ◽  
Ieva Grinfelde ◽  
Gita Taurina ◽  
Ieva Micule ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Clinical Management ◽  
Clinical Presentation ◽  
Neurodegenerative Disorder ◽  
Leigh Syndrome ◽  
Live Births ◽  
Pathogenic Variants ◽  
Associated Symptoms ◽  
Management Experience ◽  
Common Infections

Leigh syndrome is a neurodegenerative disorder with an incidence of 1 : 40,000 live births. The clinical presentation of LS is highly variable with heterogeneity in the disease-associated symptoms of cerebellar, motor, and extrapyramidal dysfunction and common infections. There is no effective treatment for this condition; as such, the prognosis of this condition is very poor with death occurring within the first few years of life. In this study, we report the first LS case in Latvia with SURF1 pathogenic variants in two siblings. The difficulties encountered establishing a diagnosis for the first proband and the effective prenatal diagnosis for the second offspring that led to termination of the pregnancy are discussed.

Prenatal diagnosis of left ventricular aneurysm in association with interruption of the aortic arch

2010 ◽  
Vol 21 (1) ◽  
pp. 113-115 ◽  
Author(s):  
Victoria Jowett ◽  
Owen Miller
Keyword(s):  
Prenatal Diagnosis ◽  
Aortic Arch ◽  
Left Ventricular ◽  
Left Ventricular Aneurysm ◽  
Ventricular Aneurysm ◽  
Pentalogy Of Cantrell ◽  
First Report

AbstractLeft ventricular aneurysms in the foetus are a rare abnormality that can occur in isolation or associated with pentalogy of Cantrell. Here, we report a case of a foetus with a left ventricular aneurysm in association with interruption of the aortic arch, and no features of pentalogy of Cantrell. To our knowledge, this is the first report of such an association.

scholarly journals Prenatal ultrasound diagnosis of fetal giant left ventricular aneurysm： A case report

2021 ◽  
Author(s):  
Wenjing Guo ◽  
Dengcai Zhang ◽  
Tingting Yao ◽  
Bin Ma ◽  
Tian-gang Li
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Rare Case ◽  
Left Ventricular ◽  
Left Ventricular Aneurysm ◽  
Ventricular Aneurysm ◽  
Prenatal Ultrasonography ◽  
Cardiac Malformation ◽  
Congenital Cardiac Malformation ◽  
Ultrasound Technology

Fetal ventricular aneurysm is a rare congenital cardiac malformation that can occur in various cardiac cavities and often exists in isolation without other malformations. Modern ultrasound technology can assist the prenatal diagnosis of ventricular aneurysm. Herein, we will present a rare case of a giant left ventricular aneurysm detected by prenatal ultrasonography.

Sign in / Sign up

Export Citation Format

Share Document