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Branchio-Oto-Renal Syndrome

More information in Books or onNLM PubMed
Definition: 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)      Other names Syndromes, Branchiooculofacial; Syndromes, Branchio-Otorenal; Syndromes, Branchio-Oto-Renal; Syndromes, Branchio-Oculo-Facial; Syndromes, BOR; Syndrome, Branchiooculofacial; Syndrome, Branchio-Otorenal; Syndrome, Branchio-Oto-Renal; Syndrome, Branchio-Oculo-Facial; Syndrome, BOR; Lip Pseudocleft Hemangiomatous Branchial Cyst Synd; Dysplasias, Branchio-Otorenal; Dysplasia, Branchio-Otorenal; Branchiooculofacial Syndromes; Branchio-Otorenal Syndromes; Branchio-Otorenal Dysplasias; Branchio-Oto-Renal Syndromes; Branchio-Oculo-Facial Syndromes; Branchio Otorenal Syndrome; Branchio Otorenal Dysplasia
 
SubstanceCAS Registry & nameCategoriesSource
Branchiootorenal syndrome 1  0   *Branchio-Oto-Renal Syndrome.
Branchiootic syndrome  0   *Branchio-Oto-Renal Syndrome.
Bor-Duane hydrocephalus contiguous gene syndrome  0   *Duane Retraction Syndrome *Hydrocephalus *Branchio-Oto-Renal Syndrome Carpal Bones/abnormalities.
NDUFB9 protein, human  EC 1.6.5.3   *NADH Dehydrogenase Branchio-Oto-Renal Syndrome. Hum Hered 1999 Mar;49(2)75-80:75-80

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

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