Shprintzen-Goldberg syndrome (SGS) is a very rare genetic disorder characterized by craniosynostosis, craniofacial and skeletal abnormalities, marfanoid habitus, cardiac anomalies, neurological abnormalities, and intellectual disability. The disease is MONDO_0008426 (Shprintzen-Goldberg syndrome). Also known as: Marfanoid craniosynostosis syndrome, SGS, Shprintzen Goldberg Syndrome.