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CASE REPORT
Year : 2018  |  Volume : 4  |  Issue : 1  |  Page : 44-47

Branchiootic Syndrome − Rare Case Reports of Patients With Complete Bilateral Branchial Fistulae


1 Department of ENT, Northern Railway Central Hospital, New Delhi, India
2 Department of ENT and Head & Neck Surgery, Maulana Azad Medical College and Associated Lok Nayak Hospital, New Delhi, India
3 Department of Otorhinolaryngology and Head & Neck Surgery, Maulana Azad Medical College and Associated Lok Nayak Hospital, New Delhi, India

Correspondence Address:
Divya Gupta
66, Raj Nagar, Pitam Pura, Delhi 110034
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/mamcjms.mamcjms_78_17

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Branchial arch anomalies are one of the most common congenital anomalies and are usually unilateral in nature. The bilateral occurrence of more than one anomaly is not only rare, but its presence along with hearing loss results in branchiootic syndrome, which has important clinical and genetic implications. Branchiootic syndrome is a part of the spectrum of branchiootorenal syndrome, which is a rare autosomal dominant condition with incomplete penetrance characterized by the malformations of the external, middle, and inner ear, hearing loss, branchial fistulae, and renal abnormalities. We shall be discussing two such rare cases in this article.


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