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Inherited retinal diseases, also known as IRDs, refer to a group of rare genetic disorders affecting the retina, the light-sensitive nerve layer at the back of the eye.
IRDs damage the rod and/or cone photoreceptor cells in the retina. Generally, rods help us see in dim light, while cones help with colour and central vision. There are many types of IRDs, such as retinitis pigmentosa (RP), cone-rod dystrophies (CRD) and macular dystrophies.
A study of the Singaporean population showed that between
one in 1,000 to 2,000 Singaporeans are affected by IRDs.
The symptoms experienced by individuals differ depending on the type of photoreceptors affected.
IRDs refer to a large group of genetic disorders that affect the retina. In most cases, the inherited gene defect only affects the eyes.
Sometimes, other parts of the body are also affected, and this is called
syndromic RP. An example of syndromic RP is Usher syndrome, which causes both RP and hearing loss. Other examples include Refsum, Alström and Laurence-Moon-Bardet-Biedl (LMBB) syndromes.
IRDs can be caused by one of many possible genetic changes, but they all result in a similar set of symptoms related to vision. Researchers have identified hundreds of different genetic changes that can each cause IRDs, although most IRD cases are caused by changes to one of a small number of commonly affected genes.
Genes are instructions for cells to make proteins in the body. Everyone carries two copies of each gene, one inherited from each parent. IRDs are the result of a change (mutation) in the relevant gene.
IRDs usually run in families, but the way it is passed from parents to their children varies depending on the specific genetic changes responsible for a person’s IRD.
Autosomal recessive IRDs occur when there are two faulty copies of the involved gene, one from each parent. Most IRD cases are inherited in an autosomal recessive pattern.
Autosomal recessive IRDs tend to produce signs and symptoms between 30 and 40 years of age and usually cause more severe sight loss.
Autosomal dominant IRDs occur when there is one faulty copy of the involved gene.
Autosomal dominant IRDs are generally less severe than other forms of IRD and usually result in symptoms from around 30 years of age.
In diseases with X-linked inheritance, the affected gene is located on the X chromosome. Typically, females have two X chromosomes, whilst males have one X and one Y chromosome.
Females with one affected copy and one normal copy are known as carriers.
As males only have one copy of the X chromosome gene, males with one affected copy do not have a second working copy and are therefore affected with the genetic disorder.
X-linked IRDs can result in severe vision loss, often with blindness or near-blindness by the age of 40. Many cases of IRDs occur in people without any known family history. Parents may have passed the genetic changes onto their offspring but did not develop symptoms themselves. In these cases, it may not be possible to determine how the IRD is inherited.
IRDs are diagnosed based on:
There are many different varieties of IRDs, each caused by specific changes in a patient’s DNA. As a result, the definitive diagnosis of the type of IRD for each patient requires a blood test to check which DNA change is responsible for the condition.
The general eye specialist you see initially will refer you to a retinal specialist with expertise in IRDs.
In some cases, confirmation of your genetic diagnosis may require other members of your family to also undergo genetic testing.
Following the initial diagnosis and genetic testing, IRD patients are monitored regularly for progression of the condition and the development of any complications, such as swelling of the retina, by a retinal specialist or paediatric ophthalmologist.
Patients with syndromic RP may additionally require monitoring and treatment by other specialists, such as an ear, nose and throat (ENT) doctor and genetics doctor.