DETECTION OF MICRODELETION IN CHROMOSOME 7q11.23 BY FLUORESCENT IN SITU HYBRIDIZATION TECHNIQUE AMONG AN EGYPTIAN COHORT SUSPECTED TO HAVE WILLIAMS SYNDROMRE
Marzouk, I., Kassem, H., Abd El-Mohsin, A., EL-Assi, H., Mansour, A. (2022). DETECTION OF MICRODELETION IN CHROMOSOME 7q11.23 BY FLUORESCENT IN SITU HYBRIDIZATION TECHNIQUE AMONG AN EGYPTIAN COHORT SUSPECTED TO HAVE WILLIAMS SYNDROMRE. EKB Journal Management System, 4(2), 10-11. doi: 10.21608/alexpo.2022.136156.1398
Iman M. Marzouk; Heba S. Kassem; Ali Abd El-Mohsin; Hoda H. EL-Assi; Aya Ahmed Mansour. "DETECTION OF MICRODELETION IN CHROMOSOME 7q11.23 BY FLUORESCENT IN SITU HYBRIDIZATION TECHNIQUE AMONG AN EGYPTIAN COHORT SUSPECTED TO HAVE WILLIAMS SYNDROMRE". EKB Journal Management System, 4, 2, 2022, 10-11. doi: 10.21608/alexpo.2022.136156.1398
Marzouk, I., Kassem, H., Abd El-Mohsin, A., EL-Assi, H., Mansour, A. (2022). 'DETECTION OF MICRODELETION IN CHROMOSOME 7q11.23 BY FLUORESCENT IN SITU HYBRIDIZATION TECHNIQUE AMONG AN EGYPTIAN COHORT SUSPECTED TO HAVE WILLIAMS SYNDROMRE', EKB Journal Management System, 4(2), pp. 10-11. doi: 10.21608/alexpo.2022.136156.1398
Marzouk, I., Kassem, H., Abd El-Mohsin, A., EL-Assi, H., Mansour, A. DETECTION OF MICRODELETION IN CHROMOSOME 7q11.23 BY FLUORESCENT IN SITU HYBRIDIZATION TECHNIQUE AMONG AN EGYPTIAN COHORT SUSPECTED TO HAVE WILLIAMS SYNDROMRE. EKB Journal Management System, 2022; 4(2): 10-11. doi: 10.21608/alexpo.2022.136156.1398

DETECTION OF MICRODELETION IN CHROMOSOME 7q11.23 BY FLUORESCENT IN SITU HYBRIDIZATION TECHNIQUE AMONG AN EGYPTIAN COHORT SUSPECTED TO HAVE WILLIAMS SYNDROMRE

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Article 1, Volume 4, Issue 2, June 2022, Page 10-11  XML
Document Type: Preliminary preprint short reports of original research
DOI: 10.21608/alexpo.2022.136156.1398
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Authors
Iman M. Marzouk1; Heba S. Kassem2; Ali Abd El-Mohsin1; Hoda H. EL-Assi2; Aya Ahmed Mansour email 2
1Department of Pediatrics, Faculty of Medicine, Alexandria University
2Department of Pathology (Genetics), Faculty of Medicine, Alexandria University
Abstract
Williams syndrome (WS) is a unique type of microdeletion syndromes thatcauses a wide spectrum of multisystemic clinical manifestations. Its incidence is somewhere between 1 in 7500-20000 livebirths. It results from a deletion of 1.5-1.8 megabases (Mb) in chromosome 7q11.23 that can be detected by fluorescent in situ hybridization (FISH) technique which is the gold standard for its diagnosis. WS is characterized by dysmorphicfacies, cardiovascular disease, most commonly
supravalvular aortic stenosis (SVAS), intellectual disability, a characteristic cognitive profile, and idiopathic hypercalcemia. This study was aiming to evaluate the clinical, cardiac, and biochemical aspects in a cohort of children with WS in Egypt and confirm the microdeletion by FISH technique.
AIM OF THE WORK:
1- Clinical assessment of children suspected to have WS attending the genetics clinic at Smouha Hospital University, Faculty of medicine.
Establishing molecular diagnosis for confirmation of the suspected cases by FISH technique through detection of chromosome 7q11.23 microdeletion.
Keywords
Williams syndrome (WS); fluorescent in situ hybridization (FISH); supravalvular aortic stenosis (SVAS)
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