Abstract
The Shprintzen-Goldberg syndrome is an extremely rare syndrome with a characteristic face. This is one of a group of disorders characterized by craniosynostosis and marfanoid features. The aim of this study was to present a new sporadic case of the syndrome and describe in detail the findings at the maxillofacial region.
MeSH terms
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Abnormalities, Multiple / pathology*
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Child
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Craniosynostoses / complications
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Craniosynostoses / pathology*
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Facial Bones / pathology
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Facies
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Female
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Humans
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Malocclusion, Angle Class II / etiology
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Marfan Syndrome / complications
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Marfan Syndrome / pathology*
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Micrognathism / etiology*
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Syndrome
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Tooth Abnormalities / etiology*