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Up to: Multiple congenital anomalies/dysmorphic syndrome-intellectual disability · Marfan and Marfan-related disorder · Syndromic craniosynostosis
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.
This condition has no sub-types.