Cerebral Autosomal Dominant Arteriopathy Health Feed

A dominantly inherited disorder means you only need to inherit the mutated gene from one parent to be affected. This means that if you have a child with an unaffected partner, there's still a 50% chance of your child developing the condition.
However, there are some medications in homoeopathy that may reduce the risk and help. You may reach us with the details of the mother and kids to get the best help possible.

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

General exercises: a range of motion and stretching exercises can help combat the inevitable inward movement of the limbs as muscles and tendons shorten. Limbs tend to become fixed in position, and these types of activities can help keep them mobile for longer. Standard low-impact aerobic exercises such as walking and swimming can also help slow the disease’s progression.
Breathing assistance: as the muscles used for breathing become weaker, it may be necessary to use devices to help improve...more

Hirschsprung disease is because of the absence of neurons in the rectum and colon. As you have undergone surgery ,it is better to seek the opinion of a gastroenterological surgeon.

Dear user, there is no study that shows the covid vaccine is a contraindication for g6pd deficiency. The vaccines are safe and should not have any side effects. However the strict diet and medication to be avoided have to be continues. You can consult me for more doubts regarding this online by clicking on my photo and booking an appointment however, if you found my answer helpful, please leave a positive feedback as it helps me with my practice. Thank you.

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.

A group of genetic diseases that cause progressive weakness and loss of muscle mass.
In muscular dystrophies, abnormal genes (mutations) lead to muscle degeneration.
In most cases, muscular dystrophy (md) runs in families. It usually develops after inheriting a faulty gene from one or both parents. Md is caused by mutations (alterations) in the genes responsible for healthy muscle structure and function.
The signs and symptoms consistent with muscular dystrophy are:[3]
progressiv...more

There r lots of physiotherapeutic treatment protocol for muscular dys trophy .u can get from youtube but better first consult with a physiotherapist, learn from his what to do whatever exercises he suggests .do continue at home in regular basis.

Yes stem cell therapy is an option of treatment for muscular dystrophy but the result is varied and not confirmed yet.

Does your bleeding get stopped after a while or you bleed for a long time. You need to check with your vitamin k levels.