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Shprintzen-Goldberg syndrome (SGS) is an extremely rare congenital disorder, occurring in approximately 1 in 1,000,000 individuals. A higher occurrence has been observed in males (Vieira et al. 2022). The condition was initially reported by Sugarman and Vogel in 1981 and was recognized as a distinct clinical entity by Shprintzen and Goldberg in 1982 (Shprintzen and Goldberg 1982). To date, only around 75 cases of Shprintzen-Goldberg syndrome have been reported in the medical literature (Vieira et al. 2022).

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Shprintzen-Goldberg Craniosynostosis Syndrome (SGS)

  • 动态工具书词条

  • 发表日期：

    2025年

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  • Mahsa Heidari-Foroozan,
  • Hosein Jafary

摘要

Shprintzen-Goldberg syndrome (SGS) is an extremely rare congenital disorder, occurring in approximately 1 in 1,000,000 individuals. A higher occurrence has been observed in males (Vieira et al. 2022). The condition was initially reported by Sugarman and Vogel in 1981 and was recognized as a distinct clinical entity by Shprintzen and Goldberg in 1982 (Shprintzen and Goldberg 1982). To date, only around 75 cases of Shprintzen-Goldberg syndrome have been reported in the medical literature (Vieira et al. 2022).