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What is Night blindness, congenital stationary, autosomal dominant?

What is Night blindness, congenital stationary, autosomal dominant?

  • Night blindness, congenital stationary, autosomal dominant: 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 dominantly inherited.

Night blindness, congenital stationary, autosomal dominant: Introduction

Types of Night blindness, congenital stationary, autosomal dominant:

Broader types of Night blindness, congenital stationary, autosomal dominant:

What causes Night blindness, congenital stationary, autosomal dominant?

Causes of Night blindness, congenital stationary, autosomal dominant: see causes of Night blindness, congenital stationary, autosomal dominant

What are the symptoms of Night blindness, congenital stationary, autosomal dominant?

Symptoms of Night blindness, congenital stationary, autosomal dominant: see symptoms of Night blindness, congenital stationary, autosomal dominant

Night blindness, congenital stationary, autosomal dominant: Testing

Diagnostic testing: see tests for Night blindness, congenital stationary, autosomal dominant.

Misdiagnosis: see misdiagnosis and Night blindness, congenital stationary, autosomal dominant.

How is it treated?

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

Name and Aliases of Night blindness, congenital stationary, autosomal dominant

Main name of condition: Night blindness, congenital stationary, autosomal dominant

Other names or spellings for Night blindness, congenital stationary, autosomal dominant:

hemeralopia, congenital essential, night blindness, congenital stationary, Rambusch type, CSNBAD2, CSNBAD3, night blindness, congenital stationary, Nougaret type, CSNBAD1, night blindness, congenital stationary, rhodopsin-related

Night blindness, congenital stationary, autosomal dominant: Related Conditions

Research the causes of these diseases that are similar to, or related to, Night blindness, congenital stationary, autosomal dominant:

 

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