Branchio-oto-renal syndrome (BOR) [4][5] is an autosomal dominant genetic disorder involving the kidneys, ears, and neck. It is also known as Melnick-Fraser syndrome. [2][3]

1999年3月19日 · Branchiootorenal spectrum disorder (BORSD) is characterized by malformations of the outer, middle, and inner ear associated with conductive, sensorineural, or mixed hearing impairment, branchial fistulae and cysts, and renal malformations ranging from mild renal hypoplasia to bilateral renal agenesis.

Branchiootorenal (BOR) syndrome is a condition that disrupts the development of tissues in the neck and causes malformations of the ears and kidneys. Explore symptoms, inheritance, genetics of this condition.

2018年1月17日 · Branchio-oculo-facial syndrome is a rare disorder inherited as an autosomal dominant trait. Major symptoms may include abnormal sinuses, growth delay, premature aging and an unusual facial appearance.

Branchio-oto-renal (BOR) syndrome, also known as Melnick-Fraser syndrome, is a congenital (present at birth) condition characterized by branchial arch malformations. Sometimes, it may not be noticeable at birth but will appear later on.

Branchio-oto-renal (BOR) syndrome, also known as Melnick-Fraser syndrome, is characterized by an association of: 1) branchial fistulae or cysts; 2) ear malformations, which can include the inner, middle and outer ear; and 3) renal malformations, which can range in severity from renal hypoplasia to agenesis.

Branchiootorenal (BOR) syndrome is a condition that disrupts the development of tissues in the neck and causes malformations of the ears and kidneys. The signs and symptoms of this condition vary widely, even among members of the same family.