Shprintzen-Goldberg syndrome

Disease Export to PDF
Name:
Shprintzen-Goldberg syndrome
Description:
A rare genetic disorder characterized by craniosynostosis, craniofacial and skeletal abnormalities, marfanoid habitus, cardiac anomalies, neurological abnormalities, and intellectual disability.
ORPHAcode:
2462
Synonyms:
Marfanoid craniosynostosis syndrome
SGS
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14