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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.
Micrognathia
Developmental hypoplasia of the mandible.
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PMID (PMCID)