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Review Question - QID 218678

Beckwith-Wiedemann Syndrome Etiology Associated conditions QID: 218678 (SBQ22PE.71)
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QID 218678 (Type "218678" in App Search)
A 4-year-old male is diagnosed with a congenital condition caused by a mutation in chromosome 11p15.5 that caused him to develop with characteristic traits of hemihypertrophy of his left lower extremity, macroglossia, and an omphalocele. For which of the following conditions should the boy be screened for every 3-6 months until he is 5-8 years of age given his genetic predisposition?
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