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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.
Hallux valgus
Lateral deviation of the great toe (i.e., in the direction of the little toe).
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PMID (PMCID)