Branchio-Oto-Renal Syndrome
From Wikipedia, the free encyclopedia
Branchio-Oto-Renal Syndrome (also known as branciootorenal syndrome or BOR) is an autosomal dominant genetic disorder involving the kidneys, ears, and neck. Individiduals with BOR may have underdeveloped (hypoplastic) or absent kidneys with resultant renal insufficiency or renal failure. Ear anomalies include extra openings in front of the ears (preauricular pits), extra pieces of skin in front of the ears (preauricular tags), or further malformation or absence of the outer ear (pinna). Malformation or absence of the middle ear is also possible. People with BOR may also have cysts or fistulae along the the sides of their neck corresponding to the location of the embryologic brancial clefts. BOR results from the mutation of the EYA1 gene.[1]
[edit] References
- ^ Mendelian Inheritance in Man (OMIM) 113650
 |
This genetic disorder article is a stub. You can help Wikipedia by expanding it. |
