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What is Night blindness, congenital stationary, type 1B?

What is Night blindness, congenital stationary, type 1B?

  • Night blindness, congenital stationary, type 1B: A rare inherited disorder of the retina that involves the rods of the eyes. A reduced sharpness of vision and night blindness are usually the only symptoms. The non-progressive disorder is recessively inherited and is linked to a defect at chromosome 5q35.

Night blindness, congenital stationary, type 1B: Introduction

Types of Night blindness, congenital stationary, type 1B:

Broader types of Night blindness, congenital stationary, type 1B:

What causes Night blindness, congenital stationary, type 1B?

Causes of Night blindness, congenital stationary, type 1B: see causes of Night blindness, congenital stationary, type 1B

What are the symptoms of Night blindness, congenital stationary, type 1B?

Symptoms of Night blindness, congenital stationary, type 1B: see symptoms of Night blindness, congenital stationary, type 1B

Night blindness, congenital stationary, type 1B: Testing

Diagnostic testing: see tests for Night blindness, congenital stationary, type 1B.

Misdiagnosis: see misdiagnosis and Night blindness, congenital stationary, type 1B.

How is it treated?

Doctors and Medical Specialists for Night blindness, congenital stationary, type 1B: Medical Geneticist, Ophthalmologist ; see also doctors and medical specialists for Night blindness, congenital stationary, type 1B.
Treatments for Night blindness, congenital stationary, type 1B: see treatments for Night blindness, congenital stationary, type 1B

Name and Aliases of Night blindness, congenital stationary, type 1B

Main name of condition: Night blindness, congenital stationary, type 1B

Other names or spellings for Night blindness, congenital stationary, type 1B:

CSNB1B, night blindness, congenital stationary, complete, autosomal recessive, CSNB, complete, autosomal recessive

 

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