Eyesopt

16/08/2023

15/08/2023

Healthy Eyes Are Blessings

05/09/2022

Retinoblastoma is also known as cancer in the retina. Retinoblastoma symptoms are vision loss, damage to the brain, or death

16/08/2022

In congenital glaucoma, there is a genetic birth defect in the angle of the eye. This fault hinders the discharge of the fluid "aqueous humor" from the eye.
Consequently, interocular pressure rises and it harms the optic nerve which connects the eye and brain.

Primary congenital glaucoma is a genetic birth defect in the angle of the eye causing hindrance in the discharge of aqueous humor.

27/03/2022

The crystalline lens of the eye is a transparent structure. It is responsible for the bending of light and its focusing on the retina. In congenital cataracts, the crystalline lens is cloudy by birth.

Congenital cataract has a tendency to pass down from parents to their children. Congenital cataract has various types, depending upon the area of lens clouding. If the opacity is central and blocks vision, then lens removal is necessary.

Congenital cataract is the cloudiness of the lens in the eye of infants which can lead to vision blurriness to blindness.

03/03/2022

Best disease is a type of macular dystrophy namely vitelliform macular dystrophy. The best disease affects 6 in 100000 people and passes down from generation to generation in an autosomal dominant pattern.

It is grouped with hereditary eye diseases because it causes a material build-up in the macula since birth. During the time period when the child grows into an adult, the build-up gradually enlarges. That way the macula has already been damaged beyond treatment. No remedy can reverse vision loss. The best disease affects both eyes but the extent of vision deterioration might not be the same in both eyes.

The disease shows symptoms later in life and sight loss may occur even after 50 years of life. Mutation in the gene named BEST1 causes Best disease. The best disease has no cure to date.

Best disease of the eye is also termed vitelliform macular dystrophy. It is caused by a fault in the gene. It can affect males and females.

20/02/2022

Retinoblastoma is the cancer of the light-sensitive layer of the eye. Children of age less than 5 years are more likely to develop this retinal cancer. The gene that causes Retinoblastoma is the RB1 gene. When gene alteration affects both copies of the RB1 gene, it results in retinoblastoma.

As retinoblastoma is an inherited disorder, routine eye screening of parents and siblings of the child is also necessary. Early detection is the key to preventing the child from both blindness and death.

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Retinoblastoma is also known as cancer in the retina. Retinoblastoma symptoms are vision loss, damage to the brain, or death

27/01/2022

Usher syndrome is a genetic disorder. The problem starts with deafness and further it is accompanied by retinitis pigmentosa that ends up with vision loss. As it is a hereditary eye disease, it affects multiple functions of the body like both hearing and vision.

We know that normal hearing depends upon the normal development of the ear. But, Usher Syndrome affects hearing because of the abnormal development of hair cells in the inner ear.

This leads to impairment of auditory nerves. Usher syndrome also affects vision by influencing the normal function of the retina by encouraging retinitis pigmentosa. Sometimes, the usher syndrome also affects the balance which results in deafness and blindness.

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Usher syndrome is a genetic disorder that starts with deafness and is accompanied by retinitis pigmentosa that ends up with vision loss.

08/01/2022

Leber hereditary optic neuropathy (LHON) is an X-linked hereditary eye disease. LHON causes the loss of vision firstly by painless blurriness and affects central vision. The most prominent symptom of the LHON is vision loss happening in teens or twenties. But in some rare cases, it also happened in childhood or later adulthood. This article will help you to learn more about LHON. Stay in touch with to spread awareness regarding hereditary eye diseases.

Leber hereditary optic neuropathy (LHON) is an X-linked hereditary disease that causes vision loss. This disease is inherited from mothers.

06/01/2022

Retinitis pigmentosa is a disease related to the eyes in which the person gradually experienced the decline of eyesight due to degeneration of the retina.
Researchers considered it as hereditary eye disease because of the gene mutation which is not favorable for the sight.

Retinitis pigmentosa affects the eyes in which the person gradually experienced a decline in eyesight and it has no permanent treatment.

22/12/2021

Human genes contain all the information regarding body development and working. One malfunctioning gene causes abnormal body development and results in a serious condition. Such malfunctioning genes tend to pass down from generation to generation. And they disturb the order of our body. Such conditions caused due to gene error are called hereditary diseases or disorders. When we talk about the eye, we name such diseases as hereditary eye diseases.

Human genes contain all information. If it malfunctions related to the eye and passes to generations, it can cause hereditary eye diseases.