Which of the following is NOT a common feature of Beckwith-Wiedemann Syndrome?

Beckwith-Wiedemann Syndrome is a complex genetic disorder characterized by overgrowth and various developmental abnormalities. The features often associated with this syndrome include hypoglycemia, ear creases, and macrosomia.

Hypoglycemia, or low blood sugar levels, is common in infants with Beckwith-Wiedemann Syndrome due to excessive insulin production related to the growth deregulation seen in the disorder.

Ear creases, which are typically seen as a fold or pit in the earlobe, are another recognized physical sign associated with this syndrome. They can serve as an external marker of the condition.

Macrosomia, or increased birth weight, is also a typical finding in affected individuals. Due to excessive growth factors, these infants often present larger than average at birth.

Retinal hemorrhage is not a characteristic feature of Beckwith-Wiedemann Syndrome. While it may occur in various conditions, it is not directly associated with the syndrome and typically does not form part of the clinical spectrum presented by individuals with this genetic disorder. Thus, identifying retinal hemorrhage as not commonly linked to Beckwith-Wiedemann Syndrome is essential when understanding the defining characteristics of the condition.