Branchiootorenal syndrome 2
Overview
Branchiootic syndrome 2: A rare inherited disorder characterized by branchial and ear abnormalities. The hearing loss is variable with respect to severity and age of onset. Type 2 is caused by a defect chromosome 1q31. It is similar to the branchio-oto-renal syndrome except it doesn't involve any kidney abnormalities.
Symptoms
* Branchial pit * Branchial fistula * Cup-shaped ears * Branchial anomalies * External ear anomalies
Causes
In addition to the above medical information, to get a full picture of the possible signs or symptoms of this condition and also possibly the signs and symptoms of its related medical conditions, it may be necessary to examine symptoms that may be caused by complications of Branchiootic syndrome 2, underlying causes of Branchiootic syndrome 2, associated conditions for Branchiootic syndrome 2, risk factors for Branchiootic syndrome 2, or other related conditions.
Diagnosis
The phrase "signs of Branchiootic syndrome 2" should, strictly speaking, refer only to those signs and symptoms of Branchiootic syndrome 2 that are not readily apparent to the patient.