Associated Papers
An Unusual Presentation of Barakat Syndrome: Gene Deletion at Chromosome 10p15.
Satariano M et al.
Case Reports in Nephrology, 2025
A novel frameshift variant of GATA3 (p.Ala17ProfsTer178) responsible for HDR syndrome in a Japanese family.
Hasegawa Y et al.
Endocrine Journal, 2024
Barakat syndrome diagnosed decades after initial presentation.
Spennato U et al.
Endocrinology, Diabetes & Metabolism Case Reports, 2023
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