What is Juvenile Retinoschisis?
What is Juvenile Retinoschisis?
- Juvenile Retinoschisis: An inherited eye condition where degenerative changes in the eye causes the retina to split. The severity and age of onset of symptoms can vary.
- Juvenile Retinoschisis: X chromosome recessive disorder, found nearly exclusively in males and becoming apparent around puberty. Characterized initially by a cystlike structure involving the FOVEA CENTRALIS, a peripheral retinoschisis occurs in about half the patients.
Source - Diseases Database
Juvenile Retinoschisis: Introduction
Types of Juvenile Retinoschisis:
Broader types of Juvenile Retinoschisis:
Who gets Juvenile Retinoschisis?
Gender Ratio for Juvenile Retinoschisis: Males only as it is inherited in a X-linked manner.
How serious is Juvenile Retinoschisis?
Complications of Juvenile Retinoschisis:
see complications of Juvenile Retinoschisis
What causes Juvenile Retinoschisis?
Causes of Juvenile Retinoschisis: see causes of Juvenile Retinoschisis
What are the symptoms of Juvenile Retinoschisis?
Symptoms of Juvenile Retinoschisis:
see symptoms of Juvenile Retinoschisis
Complications of Juvenile Retinoschisis:
see complications of Juvenile Retinoschisis
Onset of Juvenile Retinoschisis: Symptoms often occur during childhood or even infancy in severe cases in some patients, symptoms may not become apparent until the middle of adulthood.
Juvenile Retinoschisis: Testing
Diagnostic testing: see tests for Juvenile Retinoschisis.
Misdiagnosis: see misdiagnosis and Juvenile Retinoschisis.
How is it treated?
Treatments for Juvenile Retinoschisis:
see treatments for Juvenile Retinoschisis
Name and Aliases of Juvenile Retinoschisis
Main name of condition: Juvenile Retinoschisis
Other names or spellings for Juvenile Retinoschisis:
Retinoschisis, Juvenile, X-Linked
Source - Diseases Database