Please use this identifier to cite or link to this item: http://148.72.244.84:8080/xmlui/handle/xmlui/8762
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dc.contributor.authorAyyed Mohammed Namoos AL- Zubaidy-
dc.date.accessioned2023-11-09T16:59:07Z-
dc.date.available2023-11-09T16:59:07Z-
dc.date.issued2014-04-
dc.identifier.issnPrint ISSN 2219-9764-
dc.identifier.issnOnline ISSN 2617-8982-
dc.identifier.urihttps://djm.uodiyala.edu.iq/index.php/djm-
dc.identifier.urihttp://148.72.244.84:8080/xmlui/handle/xmlui/8762-
dc.description.abstractBackground: Hemophilia is hereditary bleeding distorted, and widespread in the world. The Objective: to identify the epidemiological characteristics of sample. Methodology: descriptive of study was conducted in genetic blood disease center in the AL-Ramadi Teaching Hospital for maternity & children during six months period of October to April (2012-2013).The data were collected by reviewing part of registered record in the center. Results: The study included (60) patients with hemophilia registered, (76,7%) was hemophilia A and (23,3%) hemophilia B. Age distribution revealed that the highest affected age group were those from age 6-15 years (33.3%). Gender distribution revealed that (88.3%) were males & (11.7%) were female. Residency distribution revealed that 65% were Rural & 35% were urban. The study showed that (56.7%) of cases were marriages among first cousins, (15%) of cases were marriages among close family or tribe & (28.3%) are marriages unrelated with family. Conclusion: from this study we can conclude that the most common is hemophilia A followed by hemophilia B & the number of newly registered cases is increasing with consanguineous marriages.en_US
dc.language.isoenen_US
dc.publisherUniversity of Diyala - College of Medicineen_US
dc.relation.ispartofseriesVol 6;Issue 1-
dc.subjecthemophiliaen_US
dc.subjectdescriptiveen_US
dc.subjectal –Ramadien_US
dc.titleDescriptive Study of Hemophilia in Al-Ramadi Cityen_US
dc.typeArticleen_US
Appears in Collections:مجلة ديالى الطبية / Diyala Journal of Medicine

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