Branchial cleft abnormality is a common congenital neck malformation in children, which is caused by the abnormal development of the gill sac or gill groove. It is mainly manifested as a cyst in the sinus tract and fistula in the neck, as well as branchio-oto-renal syndrome (BORS). As a rare autosomal dominant genetic disease, the typical manifestations of BORS are hearing loss, abnormal branchial cleft development and renal dysplasia. In this paper, a patient was admitted to the hospital for bilateral branchial cleft fistulas combined with bilateral anterior auricular fistulas, auricular appendix, auricle dysplasia, external auditory canal stenosis, and hearing loss. The patient was diagnosed with BORS, and underwent fistulectomy of the ne...
A 15 year old male with a first branchial cleft anomaly seen at the Usmanu Danfodiyo University Teac...
First branchial cleft cysts are rare and can present as a diagnostic challenge to the physician. The...
Branchio-oto-renal (BOR) syndrome is an autosomal dominant disorder in which affected individuals ma...
Branchio-oto-renal syndrome (BOR), also known as Melnick-Fraser Syndrome, is an autosomal dominant g...
Introduction Branchio-oto-renal (BOR) syndrome is an autosomal-dominant genetic condition with high...
Branchial arch anomalies are one of the most common congenital anomalies and are usually unilateral ...
Introduction Branchio-oto-renal (BOR) syndrome is an autosomal-dominant genetic condition with high ...
Anomalies of the first branchial cleft are rare congenital malformations of the head and neck, makin...
Observation: A 19-week-old patient seen in an oral dermatology clinic had small labial commissures p...
Branchial cleft anomalies are rare congenital malformations that result from the abnormal persistenc...
Introduction: First branchial cleft anomalies manifest with duplication of the external auditory can...
Type 2 branchial cleft anomalies are the most common cause of lateral neck swelling. We report two c...
Item does not contain fulltextOBJECTIVE: To summarize the syndromic features and evaluate the presen...
OBJECTIVE: To summarize the syndromic features and evaluate the presence of inner ear anomalies in 3...
Cervico-aural [collaural fistula] fistula is rare and it accounts for less than 5% of branchial clef...
A 15 year old male with a first branchial cleft anomaly seen at the Usmanu Danfodiyo University Teac...
First branchial cleft cysts are rare and can present as a diagnostic challenge to the physician. The...
Branchio-oto-renal (BOR) syndrome is an autosomal dominant disorder in which affected individuals ma...
Branchio-oto-renal syndrome (BOR), also known as Melnick-Fraser Syndrome, is an autosomal dominant g...
Introduction Branchio-oto-renal (BOR) syndrome is an autosomal-dominant genetic condition with high...
Branchial arch anomalies are one of the most common congenital anomalies and are usually unilateral ...
Introduction Branchio-oto-renal (BOR) syndrome is an autosomal-dominant genetic condition with high ...
Anomalies of the first branchial cleft are rare congenital malformations of the head and neck, makin...
Observation: A 19-week-old patient seen in an oral dermatology clinic had small labial commissures p...
Branchial cleft anomalies are rare congenital malformations that result from the abnormal persistenc...
Introduction: First branchial cleft anomalies manifest with duplication of the external auditory can...
Type 2 branchial cleft anomalies are the most common cause of lateral neck swelling. We report two c...
Item does not contain fulltextOBJECTIVE: To summarize the syndromic features and evaluate the presen...
OBJECTIVE: To summarize the syndromic features and evaluate the presence of inner ear anomalies in 3...
Cervico-aural [collaural fistula] fistula is rare and it accounts for less than 5% of branchial clef...
A 15 year old male with a first branchial cleft anomaly seen at the Usmanu Danfodiyo University Teac...
First branchial cleft cysts are rare and can present as a diagnostic challenge to the physician. The...
Branchio-oto-renal (BOR) syndrome is an autosomal dominant disorder in which affected individuals ma...