See what questions
a doctor would ask.
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. More detailed information about the symptoms, causes, and treatments of Branchiootic syndrome 2 is available below.
Home medical testing related to Branchiootic syndrome 2:
Read more about causes of Branchiootic syndrome 2.
Research related physicians and medical specialists:
Other doctor, physician and specialist research services:
Read about other experiences, ask a question about Branchiootic syndrome 2, or answer someone else's question, on our message boards:
Search Specialists by State and City