Townes-Brocks Syndrome Latest Advances
Find the Latest Research About Townes-Brocks Syndrome
Last Updated: 06/30/2026
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Found 147 publications
Townes-Brocks Syndrome With Consistent Renal Hypodysplasia and Variable Extrarenal Features Across Three Generations of Serbian Family.
Journal: Balkan journal of medical genetics : BJMG
Published: May 18, 2026
Townes-Brocks Syndrome as Familial Isolated Bilateral Cup Ear Deformity: A Case Report.
Journal: Clinical, cosmetic and investigational dermatology
Published: February 13, 2026
Delayed diagnosis of Townes-Brocks syndrome accompanied with kidney failure.
Journal: CEN case reports
Published: August 09, 2025
Case Report: Wide spectrum of SALL1 variants-a rare cause of pediatric chronic kidney disease.
Journal: Frontiers in pediatrics
Published: June 18, 2025
Clinical characteristics of patients with SALL1-related disorder.
Journal: Pediatric nephrology (Berlin, Germany)
Published: April 25, 2025
Molecular mechanism, diagnosis, and treatment of VACTERL association.
Journal: Frontiers in pediatrics
Published: April 10, 2025
Clinical features and novel pathogenic variants of patients with Behçet's disease like trisomy 8.
Journal: Orphanet journal of rare diseases
Published: November 14, 2024
Sall1 regulates microtubule acetylation in mesenchymal cells during mouse urethral development.
Journal: Cells & development
Published: August 05, 2024
Townes-Brocks syndrome: genotype-phenotype correlations of SALL1 variants in our series and the literature.
Journal: European journal of human genetics : EJHG
Published: July 13, 2024
A novel SALL1 C757T mutation in a Chinese family causes a rare disease --Townes-Brocks syndrome.
Journal: Italian journal of pediatrics
Published: January 30, 2024
Last Updated: 06/30/2026