BECKWITH - WIEDEMANN SYNDROME: REPORT OF TWO CASES

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MORTAZAVI H.; SHAHROKHI M.

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Paper Information

Journal: Journal of Dental School Year:2000 | Volume:18 | Issue:2 Page(s): 164-170

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Information Journal Paper

Title

BECKWITH - WIEDEMANN SYNDROME: REPORT OF TWO CASES

Author(s)

MORTAZAVI H. | SHAHROKHI M. | Issue Writer Certificate

Keywords

BECKWITH-WIEDEMANN SYNDROMEQ4

Abstract

Beckwith - Wiedemann Syndrome or partial trisomy of short arm of chromosome 11 is a rare syndrome which patients with this condition represent clinical sings such as: Macroglassia, Viscromegaly, Cardiomegaly and Wilm's tumor. This syndrome involves 1 in 13700 of all infants. Patients are usually referred to Oral and Maxillofacial Surgeons for their true macroglossia. This article represents two individual cases of B.W.S in a family.

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APA: Copy

MORTAZAVI, H., & SHAHROKHI, M.. (2000). BECKWITH - WIEDEMANN SYNDROME: REPORT OF TWO CASES. JOURNAL OF DENTAL SCHOOL SHAHID BEHESHTI UNIVERSITY OF MEDICAL SCIENCE, 18(2), 164-170. SID. https://sid.ir/paper/22019/en

Vancouver: Copy

MORTAZAVI H., SHAHROKHI M.. BECKWITH - WIEDEMANN SYNDROME: REPORT OF TWO CASES. JOURNAL OF DENTAL SCHOOL SHAHID BEHESHTI UNIVERSITY OF MEDICAL SCIENCE[Internet]. 2000;18(2):164-170. Available from: https://sid.ir/paper/22019/en

IEEE: Copy

H. MORTAZAVI, and M. SHAHROKHI, “BECKWITH - WIEDEMANN SYNDROME: REPORT OF TWO CASES,” JOURNAL OF DENTAL SCHOOL SHAHID BEHESHTI UNIVERSITY OF MEDICAL SCIENCE, vol. 18, no. 2, pp. 164–170, 2000, [Online]. Available: https://sid.ir/paper/22019/en

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