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Title

BECKWITH-WIEDEMANN SYNDROME: REPORT OF A CASE

Pages

 Start Page 2213 | End Page 2215

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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