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10.3389/fped.2021.713458

MEGDEL syndrome and SATB2-associated syndrome (SAS) are both rare congenital disorders with poor prognoses caused by gene mutations.

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10.3389/fgene.2021.692087

SATB2-associated syndrome (SAS) is an autosomal dominant neurogenetic multisystemic disorder.

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10.1111/scd.12340

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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10.3389/fnmol.2019.00033

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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10.3389/fgene.2019.00630

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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10.1097/MCD.0000000000000293

We report three brothers presenting with the SATB2-associated syndrome.

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10.3760/CMA.J.ISSN.1006-7876.2019.12.010

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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Satb2 Associated Syndrome

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Oct 03, 2022

What is/are Satb2 Associated Syndrome?

Satb2 Associated Syndrome - MEGDEL syndrome and SATB2-associated syndrome (SAS) are both rare congenital disorders with poor prognoses caused by gene mutations. ^[1] SATB2-associated syndrome (SAS) is an autosomal dominant neurogenetic multisystemic disorder. ^[2] CONCLUSION Patients with SATB2-associated syndrome have shown to have a consistent and unique set of dental findings both clinically and radiographically. ^[3] Satb2-associated syndrome (SAS) is a genetic disorder that results from the deletion or mutation of one allele within the Satb2 locus. ^[4] 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. ^[5] We report three brothers presenting with the SATB2-associated syndrome. ^[6] 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. ^[7]