Shprintzen-Goldberg syndrome

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.

Also known as: Marfanoid craniosynostosis syndrome, SGS, Shprintzen Goldberg Syndrome, Shprintzen-Goldberg syndrome, Marfanoid disorder with craniosynostosis type 1, Marfanoid disorder with craniosynostosis, type 1, Marfanoid-craniosynostosis syndrome, Shprintzen-Goldberg craniosynostosis syndrome

51 clinical trials for this condition and its sub-types.