Branchial cleft anomalies are the second most common head and neck congenital lesions in
children. It may sometimes be a part of branchio-oto-renal (BOR) syndrome, so in patients …

Introduction Branchio-oto-renal (BOR) syndrome is an autosomal-dominant genetic
condition with high penetrance and variable expressivity, with an estimated prevalence of 1 …

Branchio-oto-renal syndrome (BOR) is an autosomal dominant genetic disorder
characterized by branchial fistulas, hearing impairment, renal malformations and auricular …

Objective Establish anatomical considerations, audiological outcomes, and optimal
management in patients with branchiootic/branchiootorenal syndrome (BO/BOR). Methods …

Branchial cleft anomalies are congenital head and neck lesions that arise from incomplete
maturation of the branchial apparatus during fetal development. The branchial arches are …

Branchiootoic syndrome is part of the spectrum of brachiootorenal disorders.
Brachiootorenal disorder is a rare autosomal dominant condition, characterized by …

We describe an extremely rare case of a complete fistula, a combination of the first 2
branchial arches as a component of branchiootorenal syndrome. A 13-year-old girl …

Branchial arch anomalies can arise from the four first branchial arches, but the most
encountered cases are from the second one. Second branchial arch cysts and abscesses …

Abstract Branchio-oto-renal (BOR) syndrome is an autosomal dominant disorder
characterized by branchial arch anomalies, hearing impairment, and renal anomalies. Very …

Branchio-oto-renal (BOR) syndrome is a clinically heterogeneous autosomal dominant form
of syndromic hearing loss characterized by variable hearing impairment, malformations of …