Introduction to Satb2 Associated Syndrome
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MEGDEL syndrome and SATB2-associated syndrome (SAS) are both rare congenital disorders with poor prognoses caused by gene mutations.
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SATB2-associated syndrome (SAS) is an autosomal dominant neurogenetic multisystemic disorder.
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CONCLUSION
Patients with SATB2-associated syndrome have shown to have a consistent and unique set of dental findings both clinically and radiographically.
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Satb2-associated syndrome (SAS) is a genetic disorder that results from the deletion or mutation of one allele within the Satb2 locus.
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1 have been associated with the autosomal dominant SATB2-associated syndrome (SAS), which is still short of comprehensive diagnosis technologies for small deletions and low-level mosaicism.
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We report three brothers presenting with the SATB2-associated syndrome.
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Methods
Clinical data of one case of SATB2-associated syndrome diagnosed in Children′s Hospital Affiliated to Zhengzhou University in January 2018, were collected including clinical test, treatment plan, follow-up outcomes.
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