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Case Reviews for Two Families With Unique Variants in TBX22 Causing Abruzzo-Erickson Syndrome
Kamerin Smith1,2, Michael A Abruzzo3, Robert P Erickson4
1Health Science Center at Fort Worth, The University of North Texas, Fort Worth, Texas, USA.
American Journal of Medical Genetics. Part A
|February 3, 2026
Summary
Pathogenic variants in the T-Box Transcription Factor 22 gene (TBX22) cause Abruzzo-Erickson Syndrome (ABERS). This study found overlapping phenotypes in two families with different TBX22 variants, suggesting gain-of-function mutations cause ABERS.
Area of Science:
- Genetics
- Developmental Biology
- Medical Genetics
Background:
- Pathogenic variants in the T-Box Transcription Factor 22 gene (TBX22) are associated with X-linked cleft palate (CPX) and Abruzzo-Erickson Syndrome (ABERS).
- Understanding the phenotypic spectrum and genetic underpinnings of ABERS is crucial for diagnosis and management.
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