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Retinitis Pigmentosa

Retinitis Pigmentosa in Pregnancy

Retinitis Pigmentosa Symptoms
Retinitis Pigmentosa Treatment
Retinitis Pigmentosa Research
Retinitis Pigmentosa Picture
Retinitis Pigmentosa and Usher Syndrome
Congenital Deafness and Retinitis Pigmentosa
Retinitis Pigmentosa in Pregnancy
Genetics and Retinitis Pigmentosa
Retinitis Pigmentosa History
Stem Cell and Retinitis Pigmentosa
Retinitis Pigmentosa Foundation
Eye Chip for Retinitis Pigmentosa
Retinitis Pigmentosa Effects
CMV Retinitis
Cytomegalovirus Retinitis
Macular Degeneration

What do we know about heredity and Retinitis Pigmentosa?

Since RP is an inherited disorder, it can potentially affect another member of the family. With retinal cells being among the most specialized cells in the human body, they depend on a number of unique genes to create vision. A disease-causing mutation in any one of these genes can lead to vision loss. Researchers have discovered over 100 genes that can contain mutations leading to retinitis pigmentosa. Approximately 50 percent of RP cases are isolated and have no previous family history. The cause of these cases cannot be explained. Other cases of RP, where family history has been determined, fall into three main categories: autosomal recessive, autosomal dominant, and X-linked recessive.

Autosomal recessive RP occurs when both parents are unaffected carriers of the same defective gene. The chances of a child being affected is one in four. This means the affected child must inherit the defective gene from each parent. The chances of a parent having an unaffected child who would be a carrier of the defective gene is one in two. The chance of parents having a child completely free of the RP gene is one in four.

In autosomal dominant RP, the disease is present in males or females only when a single copy of the gene is defective. Typically, one of the parents is affected by the disease. The chance is one in two of any given offspring being affected by the disease, if the affected parent has one normal and one defective gene.

X-linked recessive RP may occur in offspring in two ways. The fathers can be affected or mothers can be carriers of the defective gene. If the father is affected, all sons will be unaffected and all daughters will be carriers. If the mother is the carrier, 1 in 2 sons will be affected and 1 in 2 daughters will be carriers. In families with the X-linked type, only males are affected, while females carry the genetic trait but do not experience serious vision loss.

What Everyone Should Know About Retinitis Pigmentosa