Mutations in three genes, EYA1, SIX1, and SIX5, are known to cause branchiootorenal syndrome. About 40 percent of people with this condition have a ...
Branchio-oto-renal (BOR) syndrome is a rare disorder inherited as an autosomal dominant genetic trait. This disorder is characterized by pits or ear tags ...
Branchio-oto-renal syndrome (BOR), also known as branchiootorenal syndrome or BOR syndrome, is an autosomal dominant genetic disorder involving the kidneys, ears, and ...
Branchio-Oto-Renal Syndrome information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis.
1. J Nephrol. 2003 Jul-Aug;16(4):603-5. Branchio-oto-renal syndrome. Rodríguez Soriano J(1). Author information: (1)University of the País Vasco ...
Related Disorders. Symptoms of the following disorders can be similar to those of branchio-oto- renal syndrome. Comparisons may be useful for a differential diagnosis:
Most people with branchio-oto-renal syndrome have some type of hearing loss. The hearing loss may be due to nerve damage (sensory), blockage of sound waves ...
Branchio-oto-renal (BOR) syndrome is an autosomal dominant disorder with branchial, otologic, and renal manifestations. The branchial manifestations usually are
Branchio-oto-renal Syndrome. Danielle Mercer 1, Fern Tsien 2, and Barbara Gordon-Wendt 1. 1 Department of Communication Disorders, LSUHSC School of Allied Health ...
A collection of disease information resources and questions answered by our Genetic and Rare Diseases Information Specialists for Branchiootorenal syndrome