Background and Aims: Congenital heart defects (CHD) are the most common type of congenital disability. Copy number variations (CNVs) have been found as one of the genetic etiology of non-syndromic CHD, and researchers have detected several pathogenic CNVs in patients with cardiac defects. Materials and Methods: In the present study, 70 patients with familial (20 patients) and sporadic (50 pati...

background: socket preservation after tooth extraction is one of the indications of bone grafting to enhance preorthodontic condition. the aim of this study is to determine the effects of socket preservation on the immediate tooth movement, alveolar ridge height preservation and orthodontic root resorption. materials and methods: in a split-mouth technique, twelve sites in three dogs were inves...

purpose: to determine the prevalence of various types of visual field defects in patients with open angle glaucoma at the time of diagnosis. methods: this cross-sectional study was performed on patients who were referred to our glaucoma clinic. open angle glaucoma was confirmed by intraocular pressure measurement, perimetry, fundoscopic examination and gonioscopy. the last perimetry of patients...

In this paper, a photonic crystal waveguide with point defects and lattice constant perturbations of +5%, -5% are being investigated. Firstly waveguide structures with constant and specific parameters are being studied and photonic band gap diagrams for TE/TM modes are depicted; then pulse propagation in the frequencies available in the band gap are shown. After that, effects of parameters like...

The effect of proof over-pressure on pressure vessels structural integrity is analysed. Risk based approach applied using Failure Analysis Diagramme to assess likelihood failure. Special attention paid crack-like defects detected by NDT regular testing which are unacceptable standards, but difficult be repaired. It was show, two examples, that such can remain if some strict conditions fulfilled...

The 22q11.2 microdeletion syndrome is one of the common microdeletion syndromes seen among children with Congenital Heart Defects. Population based studies have shown the prevalence of 22q11.2 microdeletion syndrome range from 1 in 4000 to 1 in 6000 live births.1,2 Over 80% of children with 22q11.2 microdeletion syndrome have Congenital Heart Defects.1,3,4 Diagnosis of 22q11.2 microdeletion syn...