Final answer:
Beckwith-Wiedemann syndrome (BWS) is suspected with neonatal hypoglycemia, macroglossia, large size, visceromegaly, omphalocele, and characteristic earlobe crease.
Step-by-step explanation:
The syndrome that is suspected with neonatal hypoglycemia, macroglossia, large size, visceromegaly, omphalocele, and characteristic earlobe crease is Beckwith-Wiedemann syndrome (BWS).Beckwith-Wiedemann syndrome is a rare genetic disorder characterized by overgrowth, macroglossia or enlarged tongue, organ enlargement (visceromegaly), abdominal wall defects (such as omphalocele), and distinctive earlobe crease. Other symptoms may include neonatal hypoglycemia (low blood sugar), birth defects affecting the muscles and bones, and an increased risk of childhood cancers.