| Literature DB >> 23120453 |
Mohan Kameswaran1, R S Anand Kumar, Sathiya Murali, S Raghunandhan, K Karthikeyan.
Abstract
Branchio-oto-renal syndrome (Melnick-Fraser Syndrome) is a rare Autosomal Dominant disorder characterized by the syndromic association of branchial cysts or fistulae along with external, middle & inner malformations and renal anomalies. Incomplete penetrance and variable expressivity are common with the phenotypic variation ranging from mild to severe forms & consisting of various eye, ear, oral and craniofacial abnormalities. Mutations in the EYA1 gene on chromosomal site 8q13.3 are identified as the primary cause of BOR syndrome. We present a 3year old child with BOR syndrome, who came to us with bilateral low set, malformed ears & profound cochlear hearing loss along with bilateral branchial fistulae & unilateral renal agenesis. This child underwent successful cochlear implantation recently. The clinical presentation, pre-operative investigations, intra-operative findings & post-op habilitation status are presented with special highlights on the unique facial nerve course along with middle and inner ear anomalies which posed a surgical challenge during cochlear implantation.Entities:
Keywords: Branchio-oto-renal syndrome; Renal EYA1 gene; facial nerve anomaly
Year: 2007 PMID: 23120453 PMCID: PMC3452117 DOI: 10.1007/s12070-007-0081-7
Source DB: PubMed Journal: Indian J Otolaryngol Head Neck Surg ISSN: 2231-3796