Results 11 to 20 of about 72,878 (216)

Abnormalities of fetal rib number and associated fetal anomalies using three dimensional ultrasonography

The Egyptian Journal of Radiology and Nuclear Medicine, 2014
Aim: To determine incidence of abnormal number of fetal ribs and its association with other fetal anomalies using 3D ultrasonography. Materials and methods: A prospective study conducted on 188 singleton pregnant women searching for fetal anomalies ...
Sameh Ahmad Khodair, Omar Ahmad Hassanen
doaj   +1 more source

Evaluation of macular thickness change after inferior oblique muscle recession surgery

Indian Journal of Ophthalmology, 2014
Purpose: This study aimed to evaluate the changes in macular thickness following inferior oblique muscle recession surgery. Materials and Methods: Thirty-eight eyes from 21 patients undergoing ocular muscle surgery were included.
Ece Turan-Vural, Cihan Unlu, Gurkan Erdogan, Aslan Aykut, Huseyin Bayramlar, Fatih Atmaca   +5 more
doaj   +1 more source

Evaluation of pars plana sclera fixation of posterior chamber intraocular lens

Indian Journal of Ophthalmology, 2014
Purpose: The purpose of this study was to evaluate the clinical efficacy and safety of modified posterior chamber intraocular lens (PCIOL) implantation with transscleral fixation.
Fangju Han, Wei Liu, Xiangwei Shu, Ruili Tan, Qiang Ji, Xiangjuan Zhai   +5 more
doaj   +1 more source

Scleral buckle infection with Alcaligenes xylosoxidans

Indian Journal of Ophthalmology, 2014
We describe a rare case of extraocular inflammation secondary to scleral buckle infection with Alcaligenes xylosoxidans. A 60-year-old female with a history of retinal detachment repair with open-book technique of scleral buckling presented with purulent
Chih-Kang Hsu, Yun-Hsiang Chang, Jiann-Torng Chen   +2 more
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To evaluate stereoacuity in patients with acquired esotropia and to determine factors associated with favourable outcomes

Indian Journal of Ophthalmology, 2014
Aim: To evaluate stereoacuity in patients with acquired esotropia and determine the factors associated with favorable outcomes. Materials and Methods: A total of 68 subjects aged 6 years and above were included in the study.
Monisha E Nongpiur, Anirudh Singh, Rohit Saxena, Anudeepa Sharma, Pradeep Sharma   +4 more
doaj   +1 more source

Immunohistochemical features of the structure of fetuses’ uterus with a gestational term of 21-28 weeks from mothers, whose pregnancy is complicated by chronic infection of the lower genital tract

Journal of Education, Health and Sport, 2021
The relevance of the following article is prescribed by the growing number of perinatal mortality and morbidity among newborns due to the mother’s chronic infection of the lower genital tract (HILGT).
V. O. Polyasnyi, L. S. Kupriianova
doaj   +1 more source

23-gauge vitrectomy with intraocular foreign body removal via the limbus: An alternative approach for select cases

Indian Journal of Ophthalmology, 2014
Purpose: To study the outcome of removal of retained intraocular foreign bodies (RIOFBs) via limbus using 23-gauge transconjunctival sutureless vitrectomy (TSV).
Ramandeep Singh, Swapnil Bhalekar, Mangat R Dogra, Amod Gupta   +3 more
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Prenatal Diagnosis of 17p11.2 Copy Number Abnormalities Associated With Smith–Magenis and Potocki–Lupski Syndromes in Fetuses

Frontiers in Genetics, 2021
Smith-Magenis syndrome and Potocki-Lupski syndrome are rare autosomal dominant diseases. Although clinical phenotypes of adults and children have been reported, fetal ultrasonic phenotypes are rarely reported.
Meiying Cai, Xianguo Fu, Liangpu Xu, Na Lin, Hailong Huang   +4 more
doaj   +1 more source

Analysis of autosomal dominant genes impacted by copy number loss in 24,844 fetuses without structural abnormalities

BMC Genomics, 2022
Background The broad application of high-resolution chromosome detection technology in prenatal diagnosis has identified copy number loss (CNL) involving autosomal dominant (AD) genes in certain fetuses.
Lin Chen, Li Wang, Daishu Yin, Feng Tang, Yang Zeng, Hongmei Zhu, Jing Wang   +6 more
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Clinical Utility and the Yield of Single Nucleotide Polymorphism Array in Prenatal Diagnosis of Fetal Central Nervous System Abnormalities

Frontiers in Molecular Biosciences, 2021
Applying single nucleotide polymorphism (SNP) array to identify the etiology of fetal central nervous system (CNS) abnormality, and exploring its association with chromosomal abnormalities, copy number variations, and obstetrical outcome.
Meiying Cai, Hailong Huang, Liangpu Xu, Na Lin   +3 more
doaj   +1 more source