EVALUATION OF CRANIOFACIAL ABNORMALITY IN THALASSEMIC PATIENTS WHO REFERRED TO ALI ASGHAR HOSPITAL

Q: How can I download an article?

To download an article from SID, first log in to the site, search for the article title, and click on the 'Download Article' option.

Q: How can I download an ISI article?

To download an ISI article on SID, enter the keyword or article title in the search bar, view the relevant results, click on the desired article, and select the 'Download Article' option.

Q: How can I access the SID database?

To access the SID database, visit SID.ir, create an account, and log in to access scientific resources.

Q: Is downloading articles from SID free?

Some articles on SID are available for free, while others require payment. Details are specified on the article's page.

AGHA HOSSEINI F.; SHANBADI M.

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Journal Paper

Paper Information

Journal: Journal of Dental Medicine Year:2000 | Volume:13 | Issue:2 (24) Page(s): 16-24

Download Full-Text

Persian Verion

View:

784

Download:

Cites:

Information Journal Paper

Title

EVALUATION OF CRANIOFACIAL ABNORMALITY IN THALASSEMIC PATIENTS WHO REFERRED TO ALI ASGHAR HOSPITAL

Author(s)

AGHA HOSSEINI F. | SHANBADI M. | Issue Writer Certificate

Keywords

THALASSEMIAQ4

CRANIOFACIALQ4

CLASS II MALOCCLUSIONQ4

Abstract

THALASSEMIA syndromes are the most common single gene abnormality. It is transmitted by autosomal dominant or autosomal co- dominant genes, either homozygous (THALASSEMIA major) or heterozygous (THALASSEMIA minor). The most severe form of congenital hemolytic anemia in Iran is homozygous type. As a result, considering the recognition, complication of this disease seems necessary.This cross-sectional study has performed on 98 thalassemic patients who received transfusion therapy monthly in Ali Asghar hospital. These patients have been evaluated from the point of CRANIOFACIAL abnormality, providing answer sheet. Also, the levels of CBC and hemoglobin were determined in these patients and considered whether they were carriers or not. In this study, the incidence of deep-bite was 48% in all cases and 52.2 percent Cl II malocclusion.This findings show that transfusion therapy would diminish or, indeed, prevent development of bony abnormality in growing patients. Also, the least CRANIOFACIAL abnormality found when the mean level of hemoglobin was optimal.

Cites

References

بررسی بتا تالاسمی ماژور و تغییرات استخوانی صورت و دندانها در 50 بیمار مبتلا

Cite

APA: Copy

AGHA HOSSEINI, F., & SHANBADI, M.. (2000). EVALUATION OF CRANIOFACIAL ABNORMALITY IN THALASSEMIC PATIENTS WHO REFERRED TO ALI ASGHAR HOSPITAL . JOURNAL OF DENTAL MEDICINE, 13(2 (24)), 16-24. SID. https://sid.ir/paper/25335/en

Vancouver: Copy

AGHA HOSSEINI F., SHANBADI M.. EVALUATION OF CRANIOFACIAL ABNORMALITY IN THALASSEMIC PATIENTS WHO REFERRED TO ALI ASGHAR HOSPITAL . JOURNAL OF DENTAL MEDICINE[Internet]. 2000;13(2 (24)):16-24. Available from: https://sid.ir/paper/25335/en

IEEE: Copy

F. AGHA HOSSEINI, and M. SHANBADI, “EVALUATION OF CRANIOFACIAL ABNORMALITY IN THALASSEMIC PATIENTS WHO REFERRED TO ALI ASGHAR HOSPITAL ,” JOURNAL OF DENTAL MEDICINE, vol. 13, no. 2 (24), pp. 16–24, 2000, [Online]. Available: https://sid.ir/paper/25335/en

Related Journal Papers