BECKWITH-WIEDEMANN SYNDROME: REPORT OF A CASE

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BOZORGMEHR BITA; MOHAMMADI MARYAM; KARIMINEJAD ARIANA

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Journal: GENETICS IN THE 3RD MILLENNIUM Year:2011 | Volume:8 | Issue:4 Page(s): 2213-2215

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Information Journal Paper

Title

BECKWITH-WIEDEMANN SYNDROME: REPORT OF A CASE

Author(s)

BOZORGMEHR BITA | MOHAMMADI MARYAM | KARIMINEJAD ARIANA | Issue Writer Certificate

Keywords

BECKWITH-WIEDEMANN SYNDROMEQ3

MACROGLOSSIAQ3

MENTAL RETARDATIONQ3

Abstract

BECKWITH-WIEDEMANN SYNDROME is a disorder characterized at birth by macrosomia, MACROGLOSSIA, hypoglycemia and omphalocele. It is one of the causes of MENTAL RETARDATION. The gene is on the 11p15. We are reporting a 21-month-old boy with moderate MENTAL RETARDATION, a prominent occiput, MACROGLOSSIA, crease of ear lobule and auricular pits. We believe that our patient is a new case of BECKWITH-WIEDEMANN SYNDROME.

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APA: Copy

BOZORGMEHR, BITA, MOHAMMADI, MARYAM, & KARIMINEJAD, ARIANA. (2011). BECKWITH-WIEDEMANN SYNDROME: REPORT OF A CASE. GENETICS IN THE 3RD MILLENNIUM, 8(4), 2213-2215. SID. https://sid.ir/paper/117205/en

Vancouver: Copy

BOZORGMEHR BITA, MOHAMMADI MARYAM, KARIMINEJAD ARIANA. BECKWITH-WIEDEMANN SYNDROME: REPORT OF A CASE. GENETICS IN THE 3RD MILLENNIUM[Internet]. 2011;8(4):2213-2215. Available from: https://sid.ir/paper/117205/en

IEEE: Copy

BITA BOZORGMEHR, MARYAM MOHAMMADI, and ARIANA KARIMINEJAD, “BECKWITH-WIEDEMANN SYNDROME: REPORT OF A CASE,” GENETICS IN THE 3RD MILLENNIUM, vol. 8, no. 4, pp. 2213–2215, 2011, [Online]. Available: https://sid.ir/paper/117205/en

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