Zobrazeno 1 - 10
of 68
pro vyhledávání: '"Anita Kaul"'
Publikováno v:
BMC Pregnancy and Childbirth, Vol 21, Iss 1, Pp 1-7 (2021)
Abstract Background To evaluate the performance of the Fetal Medicine Foundation (FMF) preterm preeclampsia (PE) screening algorithm in an indigenous South Asian population. Methods This was a prospective observational cohort study conducted in a ter
Externí odkaz:
https://doaj.org/article/0d6bc5e706ac4b50b1820f2dab0494f7
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 26, Iss 3, Pp 162-169 (2021)
Introduction: Isolated fetal ascites is an uncommon finding, and it may be difficult to elucidate the underlying pathology. This is more so when there are limited resources to investigate the patient adequately. This study was undertaken to see the e
Externí odkaz:
https://doaj.org/article/8285cdabb0164c88840edf25c15da405
Publikováno v:
Indian Journal of Radiology and Imaging, Vol 29, Iss 04, Pp 448-451 (2019)
Most of the fetal deformities are caused due to genetic abnormalities. Although magnetic resonance imaging (MRI) may be used to accurately diagnose these deformities, it has been reported that gene analysis is a more accurate diagnostic method. Harle
Externí odkaz:
https://doaj.org/article/37d2a254da8c499881e5db1c83329052
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 11, Iss 2, Pp QJ01-QJ02 (2017)
Externí odkaz:
https://doaj.org/article/f294c7e603c042cb909d9992fd0b9fe9
Publikováno v:
Asian Journal of Transfusion Science, Vol 9, Iss 2, Pp 210-212 (2015)
Anti-G has been reported as a possible cause of hemolytic disease of the fetus and newborn (HDFN), either independently or in association with anti-D, anti-C or both. The antibody mimics the pattern of anti-C and anti-D reactivity in the identificati
Externí odkaz:
https://doaj.org/article/25c9f43be5644a5f89ce1b0aa479a245
Publikováno v:
Case Reports in Genetics, Vol 2013 (2013)
Peters’ plus syndrome is a rare but clinically recognizable autosomal recessive ocular genetic syndrome. Diagnosis during the fetal life is challenging due to the presence of nonspecific findings such as ventriculomegaly in the growth-retarded fetu
Externí odkaz:
https://doaj.org/article/b03ae0345ca5440daa7450c5bb9ed48b
Publikováno v:
Journal of Ultrasound in Medicine. 41:2877-2883
Autor:
Akshatha Sharma, Anita Kaul
Publikováno v:
Archives of Gynecology and Obstetrics.
Several congenital abnormalities present late in pregnancy necessitating invasive testing to rule out genetic/infectious causes at late gestation. Not many studies have described the indications/safety of a late gestation amniocentesis.All records of
Publikováno v:
The Indian journal of medical research. 154(5)
Down syndrome (DS) is one of the most common causes of developmental delay. In India, there is no protocol for prenatal screening of DS. Second-trimester biochemical screening is still being done by triple test. Quadruple test is with better sensitiv
Publikováno v:
Fetal Diagnosis and Therapy. 48:272-278
Objectives: Our study aimed to examine a subset of electively reduced twins and compare their outcomes with those of expectantly managed twins, along with a cohort of singleton pregnancies. The secondary aim was to ascertain the procedure-related mis