Cerebral Amyloid Angiopathy Health Feed

I am sorry to hear about your concern but will be happy to assist you.
Most people with autosomal dominant retinitis pigmentosa have an affected parent and other family members with the disorder.
Let's connect over a call so that we can discuss your concern in details and make a suitable treatment plan for you.

Although there is no cure for rp, treatments are available for managing some aspects of its clinical manifestations. New treatments involving gene therapy, transplantation, and implanted electrical devices, are in active development.

I am sorry to hear about your concern but will be happy to assist you.
The length of time phn lasts also varies. Many patients report symptoms lasting from one to three months, but some patints may experience symptoms up to a year or longer.
Let's connect over a call so that we can discuss your concern in details and make a suitable treatment plan for you.

Hi. Unfortunately there is no cure for rp as on now. All the medications or inventions are just aimed at improving the already diminished vision or improving the quality of life. For you per se genetic testing isn’t much useful now that you already have the disease.
But you should definitely get the genetic testing and counselling of your partner before marriage. Meanwhile, advise for you - 1. Vit a supplements 2. Visit an eye doctor if you experience further drop in your vision as there m...more

In most cases, the retinitis pigmentosa is linked to a recessive gene, a gene that must be inherited from both parents in order to cause the disease. But we have to look into the details of the problem. Let's have a detailed discussion to ensure proper treatment.

Osteogenesis Imperfecta (OI) is a group of genetic disorders that primarily affect the bones, making them extremely weak. It is also known as brittle bones disease . This genetic disease is incurable and the treatment is primarily focused on pacifying the condition by reducing pain and strengthening the bones.

The symptoms of OI include, but are not limited to, recurring fractures, bluish tinge in the white of the eyes, hearing loss, breathing problems, short height, loose joints and d...more

Dear it is genetic disorder
we have to adjust in life.
Learn how to live happily.
We have two such friends living near my residence doing well. Contact genetic counceller.

AS YOU KNOW IT IS GENETIC DISORDER.
THERE IS NO TREATMENT.
WE HAVE TO ADJUST LIFE STYLE.
COUNCELLING IS REQUIRED

Yes vitamin a is very essential for vision but in normal condon.
In case if a disease proper treatment is required with that.

Hi, Lybrate user, exact valve affected be pointed out inorder to begine homoeo medication, properly.
Related report be needed, privetly in this regard, please, till then, tk, homoeopathic medicine, underlying:
@ crategus oxq -10 drops with little water ,thrice.
Tk, care.