branchiootorenal syndrome

An uncommon (1:40:000) autosomal dominant MIM 113650 condition characterised by mixed hearing loss accompanied by a Mondini-type cochlear malformation, bilateral renal dysplasia with abnormalities of collecting ducts and bilateral branchial clefts and/or cysts.

bran·chi·o·ot·o·re·nal syn·drome

(brang'kē-ō-ō'tō-rē'năl sin'drōm) An autosomal dominant disorder characterized by anomalies of the pharyngeal arch (branchial arch) derivatives, sensory hearing impairment, and renal abnormalities.

单词	branchiootorenal syndrome
释义	branchiootorenal syndrome branchiootorenal syndrome An uncommon (1:40:000) autosomal dominant MIM 113650 condition characterised by mixed hearing loss accompanied by a Mondini-type cochlear malformation, bilateral renal dysplasia with abnormalities of collecting ducts and bilateral branchial clefts and/or cysts. bran·chi·o·ot·o·re·nal syn·drome (brang'kē-ō-ō'tō-rē'năl sin'drōm) An autosomal dominant disorder characterized by anomalies of the pharyngeal arch (branchial arch) derivatives, sensory hearing impairment, and renal abnormalities.
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