Please use this identifier to cite or link to this item: https://repository.sustech.edu/handle/123456789/3388
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dc.contributor.authorIbrahim, Mariam Abbas
dc.contributor.authorSupervisor,- Samia Mahdi Ahmed
dc.date.accessioned2014-02-06T09:15:26Z
dc.date.available2014-02-06T09:15:26Z
dc.date.issued2008-04-01
dc.identifier.citationIbrahim,Mariam Abbas.The Value of Molecular Analysis Using SRY and Amelogenin Genes in Sex Determination among Patients with Sex Differentiation Disorders/Mariam Abbas Ibrahim;Samia Mahdi Ahmed.-Khartoum:Sudan University of Science and Technology,college of Medical Laboratory Science,2008.-66p. : ill. ; 28cm.-M.Sc.en_US
dc.identifier.urihttp://repository.sustech.edu/handle/123456789/3388
dc.descriptionThesisen_US
dc.description.abstractFifteen patients were referred with provisional diagnosis of intersex from hospitals or private clinics of different geographical regions in Sudan to the Department of Clinical Genetics at the Radiation and Isotopes Center, Al Neelain Medical Research Center, and Elite Clinic for cytogenetic and/or molecular diagnosis. Of the 15 patients, 11 of them (73.3%) were raised as females, while 4 of them (26.7%) were raised as males; those patients were diagnosed by The Sudanese Intersex Working Group according to the medical history, physical examination, ultrasound, hormonal analysis, cytogenetic, and molecular studies. The aim of this study was to determine the value of molecular analysis using SRY and Amelogenin genes in sex determination among patients with sex differentiation disorders by detection of presence or absence of SRY gene (sex determining region on Y chromosome) and findings of amelogenin gene (amelogenin gene found in both X and Y chromosomes with different molecular weights) in association with karyotyping. Venous blood samples were taken from every patient to detect the presence or absence of SRY gene and the amelogenin gene findings compared with the karyotyping of all patients. . DNA extraction was done and then PCR (polymerase chain reaction) was held to detect the presence or absence of SRY gene and amelogenin gene findings (either indicate XX or XY chromosomes). The results of this study showed that 12 patients (80%) found to have XY karyotype, SRY positive and amelogenin findings showing XY pattern. One patient (6.7%) had XY chromosomes, SRY present, and amelogenin findings showing XX. Another patient (6.7%) resulted in XX chromosomes, SRY present, and amelogenin findings indicated presence of XY chromosomes. The last patient (6.7%) had a mosaic karyotype (XX/XY), SRY positive and the amelogenin findings showed XY pattern. These results indicated that the sex determination can never be based on the detection of amelogenin gene alone, but rather on the karyotyping and SRY gene, because the amelogenin gene never tells about mosaic conditions and SRY gene translocation, while karyotyping and SRY gene do.en_US
dc.description.sponsorshipSudan University of Science & Technologyen_US
dc.language.isoenen_US
dc.publisherSudan University of Science and Technologyen_US
dc.subjectMolecular Analysis-SRYen_US
dc.subjectAmelogenin Genesen_US
dc.subjectSex Differentiation-Disordersen_US
dc.titleThe Value of Molecular Analysis Using SRY and Amelogenin Genes in Sex Determination among Patients with Sex Differentiation Disordersen_US
dc.typeThesisen_US
Appears in Collections:Masters Dissertations : Medical Laboratory Science

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