Branchio-Oto-Renal Syndrome


BOF Syndrome

BOR Syndrome

Branchial Clefts with Characteristic Facies, Growth Retardation, Imperforate Nasolacrimal Duct, and Premature Aging

Branchio Oculo Facial Syndrome

Branchio Oto Renal Syndrome

Branchio-Oculo-Facial Syndrome

Branchio-Otorenal Dysplasia

Branchio-Otorenal Syndrome

Branchiooculofacial Syndrome

Branchiootorenal Dysplasia

Branchiootorenal Syndrome 1

Branchiootorenal Syndrome 2

Dysplasia, Branchiootorenal

Hemangiomatous Branchial Clefts Lip Pseudocleft Syndrome

Hemangiomatous Branchial Clefts-Lip Pseudocleft Syndrome

Lee Root Fenske Syndrome

Lip Pseudocleft Hemangiomatous Branchial Cyst Syndrome

Lip Pseudocleft-Hemangiomatous Branchial Cyst Syndrome

Melnick Fraser Syndrome

Melnick-Fraser Syndrome

Syndrome, BOF

Syndrome, BOR

Syndrome, Branchio-Oculo-Facial

Syndrome, Branchio-Oto-Renal

Syndrome, Branchiooculofacial

Syndrome, Melnick-Fraser

An autosomal dominant disorder manifested by various combinations of preauricular pits, branchial fistulae or cysts, lacrimal duct stenosis, hearing loss, structural defects of the outer, middle, or inner ear, and renal dysplasia. Associated defects include asthenic habitus, long narrow facies, constricted palate, deep overbite, and myopia. Hearing loss may be due to Mondini type cochlear defect and stapes fixation. (Jablonski's Dictionary of Syndromes & Eponymic Diseases, 2d ed)