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  The Cain Foundation Forum  Discussion Topi...  General   BRANCHIO-OTO-RENAL SYNDROME
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New Post 2/28/2018 8:28 PM
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Is an autosomal dominant genetic disorder involving kidneys, ear and nek . individual with BOR may have underdeveloped ( hypoplastic ) or absent kidnrys with resultant renal insufficiency or renal faliure.
ear anomalies include extra opening in front of the ears ( preauricular pits) , extra pieces of skin in front of the ear ( preauricular tags) or furthur malformation or absence of the outer ear ( pinna) .
individuals can have mild to profound hearing loss, which can either sensorineural , conductive or mixed.people withBOR may also have cysts or fistula along the sides of their neck corresponding to the location of the embryologic brachial clefts.

Any help appreciated.


I didn't find the right solution from the Internet.



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  The Cain Foundation Forum  Discussion Topi...  General   BRANCHIO-OTO-RENAL SYNDROME



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