![]() Treatment for Juvenile RetinoschisisĪs with retinitis pigmentosa, there is currently no treatment available for juvenile retinoschisis. During the patient’s 50s or 60s, their vision will likely start declining again at a significant rate. Vision first declines during childhood but then normalizes in early adulthood. ![]() Juvenile retinoschisis often occurs in two waves. Some other symptoms in infants and very young children can include: Juvenile retinoschisis is generally detected when the affected child has difficulty reading or exhibits other signs of poor vision. In retinoschisis, the proteins responsible for organizing retinal cellular structure do not function properly, which results in the retina splitting into two layers. The overwhelming vast majority of cases occur in male children. Juvenile retinoschisis is a rare vision disorder that is caused by a recessive genetic mutation carried on the X chromosome. Retinitis pigmentosa, and many other inheritable retinal conditions, are heavily studied, so there is always the possibility of a new treatment being developed in the near future. There are also low vision aids and rehabilitation services that can help patients with retinitis pigmentosa lead a fulfilling and active life. However, nutritional supplements such as Vitamin A can potentially help slow the disease’s progression.
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