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What is Branchio-oto-renal (BOR) syndrome, type 2?

What is Branchio-oto-renal (BOR) syndrome, type 2?

  • Branchio-oto-renal (BOR) syndrome, type 2: A rare genetic disorder characterized by abnormal kidney development and varying degrees of hearing impairment. Type 2 involves a defect on the SIX5 gene on chromosome 19q13.3.

Branchio-oto-renal (BOR) syndrome, type 2: Introduction

Types of Branchio-oto-renal (BOR) syndrome, type 2:

Broader types of Branchio-oto-renal (BOR) syndrome, type 2:

What causes Branchio-oto-renal (BOR) syndrome, type 2?

Causes of Branchio-oto-renal (BOR) syndrome, type 2: see causes of Branchio-oto-renal (BOR) syndrome, type 2

What are the symptoms of Branchio-oto-renal (BOR) syndrome, type 2?

Symptoms of Branchio-oto-renal (BOR) syndrome, type 2: see symptoms of Branchio-oto-renal (BOR) syndrome, type 2

Branchio-oto-renal (BOR) syndrome, type 2: Testing

Diagnostic testing: see tests for Branchio-oto-renal (BOR) syndrome, type 2.

Misdiagnosis: see misdiagnosis and Branchio-oto-renal (BOR) syndrome, type 2.

How is it treated?

Doctors and Medical Specialists for Branchio-oto-renal (BOR) syndrome, type 2: Medical Geneticist ; see also doctors and medical specialists for Branchio-oto-renal (BOR) syndrome, type 2.
Treatments for Branchio-oto-renal (BOR) syndrome, type 2: see treatments for Branchio-oto-renal (BOR) syndrome, type 2

Name and Aliases of Branchio-oto-renal (BOR) syndrome, type 2

Main name of condition: Branchio-oto-renal (BOR) syndrome, type 2

Other names or spellings for Branchio-oto-renal (BOR) syndrome, type 2:

Branchiootorenal syndrome 2

 

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