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Up to: Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
Omphalocele syndrome, Shprintzen-Goldberg type
Shprintzen-Goldberg omphalocele syndrome is a very rare inherited malformation syndrome characterized by omphalocele, scoliosis, mild dysmorphic features (downslanted palpebral fissures, s-shaped eyelids and thin upper lip), laryngeal and pharyngeal hypoplasia and learning disabilities.
This condition has no sub-types.