Anatomic survey of the fetus and early diagnosis of fetal anomalies

2014 ◽  
pp. 1-29
Keyword(s):  
Early Diagnosis ◽  
Fetal Anomalies

386: The nuchal translucency examnination leading to early diagnosis of structural fetal anomalies

2011 ◽  
Vol 204 (1) ◽  
pp. S155-S156
Author(s):  
Israel Goldstein ◽  
Boris Weizman ◽  
Ron Beloosesky ◽  
Khatib Nizar ◽  
Israel Thaler ◽  
...  
Keyword(s):  
Early Diagnosis ◽  
Nuchal Translucency ◽  
Fetal Anomalies

scholarly journals An observational study of abnormal findings in fetus during 11-13+6 weeks and targeted imaging for fetal anomalies ultrasonography

2020 ◽  
Vol 9 (8) ◽  
pp. 3428
Author(s):  
Amrita D. Patel ◽  
Janki B. Shingadia ◽  
Devang Patel
Keyword(s):  
General Population ◽  
Early Diagnosis ◽  
Observational Study ◽  
Fetal Anomaly ◽  
Structural Abnormality ◽  
Targeted Imaging ◽  
Fetal Anomalies ◽  
Fetal Abnormality ◽  
Fetal Medicine ◽  
Fetal Abnormalities

Background: Congenital anomalies are responsible for a of 14.2% of perinatal mortality in India. This study focuses on incidence of structural fetal abnormalities detected during 1st and 2nd trimester sonography. Aim of this study was to evaluate the need for targeted fetal scans.Methods: This study is an observational study conducted at Gujarat fetal medicine Centre, Ahmedabad, Gujarat, super specialty antenatal radiology centre where exclusively antenatal USGs and prenatal procedures are performed. All pregnant female coming for 1st and 2nd trimester USG were included. All fetal abnormalities in form of soft markers and structural abnormality were included.Results: Out of 2122 total ANC scans, 183 cases (8.6%) had structural abnormality and 235 cases (11%) had significant soft markers. 1185 cases (55.84%) came in late 2nd trimester for TIFFA scan and 468 (22%) were seen in 1st trimester scan. The incidence of fetal anomaly in this study was higher than general population as it is an exclusively fetal medicine centre and majority of patients were diagnosed with anomaly in late 2nd trimester.Conclusions: There is immense need for early diagnosis and timely intervention before 20 weeks in case of prenatal detection of fetal abnormality.

The nuchal translucency examination leading to early diagnosis of structural fetal anomalies

2014 ◽  
Vol 90 (2) ◽  
pp. 87-91 ◽  
Author(s):  
Israel Goldstein ◽  
Boris Weizman ◽  
Khatib Nizar ◽  
Zeev Weiner
Keyword(s):  
Early Diagnosis ◽  
Nuchal Translucency ◽  
Fetal Anomalies

scholarly journals P06.15: The nuchal translucency examination leading to early diagnosis of structural fetal anomalies

2011 ◽  
Vol 38 (S1) ◽  
pp. 187-187
Author(s):  
I. Solt ◽  
I. Goldstein ◽  
B. Weizman ◽  
K. Nizar ◽  
Z. Weiner
Keyword(s):  
Early Diagnosis ◽  
Nuchal Translucency ◽  
Fetal Anomalies

Red Flags: Barriers to Listening and Spoken Language in Children with Hearing Loss

2014 ◽  
Vol 24 (1) ◽  
pp. 11-18
Author(s):  
Andrea Bell ◽  
K. Todd Houston
Keyword(s):  
Hearing Loss ◽  
Early Diagnosis ◽  
Skill Acquisition ◽  
Dynamic Process ◽  
Spoken Language ◽  
Red Flags ◽  
Careful Monitoring ◽  
Auditory Development ◽  
Children With Hearing Loss ◽  
Family Centered

To ensure optimal auditory development for the acquisition of spoken language, children with hearing loss require early diagnosis, effective ongoing audiological management, well fit and maintained hearing technology, and appropriate family-centered early intervention. When these elements are in place, children with hearing loss can achieve developmental and communicative outcomes that are comparable to their hearing peers. However, for these outcomes to occur, clinicians—early interventionists, speech-language pathologists, and pediatric audiologists—must participate in a dynamic process that requires careful monitoring of countless variables that could impact the child's skill acquisition. This paper addresses some of these variables or “red flags,” which often are indicators of both minor and major issues that clinicians may encounter when delivering services to young children with hearing loss and their families.

Neonatal Serum Electrolyte and Proteinuria Screening on 46,XY Ambiguous Genitalia Patients May Allow Early Diagnosis of Denys-Drash Syndrome: A Case Report

Urology ◽  
2020 ◽  
Author(s):  
Angelena Edwards ◽  
Niccolo M. Passoni ◽  
Rebecca Collins ◽  
Smitha Vidi ◽  
Jyothsna Gattineni ◽  
...  
Keyword(s):  
Case Report ◽  
Early Diagnosis ◽  
Ambiguous Genitalia ◽  
Serum Electrolyte ◽  
Drash Syndrome
Sign in / Sign up

Export Citation Format

Share Document