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Genetic Disorders Questions

Is it possible in India to remove genes for diseases like cancer, myopia, and hashimoto's through genetic testing of embryos before implanting in the womb?

Is it possible in India to remove genes for diseases like cancer, myopia, and hashimoto's through genetic testing of ...
Please read the article which was published regarding the BRCA gene editing from embryos. They didnt do gene editing. It was embryo selection. So those embryos which did not have the gene were implanted. Gene editing if technically feasible, but a lot of problems with it at present. Feel free to contact me directly if you want to discuss this further.
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Sir. My friend is suffering from freidriech ataxia. I want to know that treatment for freidriech ataxia is it possible or not?

Hello, Generally, within 10 to 20 years after the appearance of the first symptoms the person is confined to a wheelchair. Individuals may become completely incapacitated in later stages of the disease. Friedreich ataxia can shorten life expectancy, and heart disease is the most common cause of death.
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Sir, My son is suffering with Hemophilia B, his percentage is below 4% his thigh bleeding internal is their any medicine for cure this disease. Always factor not available in hospitals if any medicine please suggest me sir we have 10 to 20 patients is there.

Sir,
My son is suffering with Hemophilia B, his percentage is below 4% his thigh bleeding internal is their any medic...
Hi, Hemophilia B is a genetic disease, present since birth, and only treatment is factor replacement. The factor therapy ideally should be given prophylactically, that means should be given weekly for life long so as to prevent any bleeding episodes. If factor is not readily available, then you can use factor as and when injury occurs along with prompt ice application and avoiding over the counter NSAID pain medicines. There are lots of centre both Govt and Private including our centre, where Factor is nowadays available readily free f cost. You should contact with nearest Hemophilia Society for Factor therapy. Hope it helps.
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Meri second beti ko drome syndrome hai. Agar mai third bachhe ko janam deti hu to kya usko bhi drome syndrome ho sakta hai.

Meri second beti ko drome syndrome hai. Agar mai third bachhe ko janam deti hu to kya usko bhi drome syndrome ho sakt...
Down syndrome may or may happen with your next pregnancy but after getting pregnant we can check the chromosome status before third month and plan accordingly
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Do I have klinefelter syndrome? I have little hips like a woman. But have facial and chest hair. of course with male genital. And good sex drive. I masturbate almost every week Should I have any other symptoms?

Do I have klinefelter syndrome?
I have little hips like a woman. But have facial and chest hair. of course with male ...
Klinefelter can be confirmed only by chromosomal study, there are lots of other features you have not mentioned. based on what u say alone it cannot be diagnosed. Good luck
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I have 66 million cells /ml. Do I have klinefelter syndrome. I have little hips like woman. 21 year old.

I have 66 million cells /ml. Do I have klinefelter syndrome. I have little hips like woman. 21 year old.
You are worrying unnecessarily. If it's bothering you consult a geneticist and get your chromosome pattern.
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If a wife parent is deaf and mute then what is the chances of their offspring in the case of hereditary.

Can not say for sure. She is not deaf. That matters. Go ahead and get married. Genetics is a complex science.
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Hi sir, Please tell me about the effect of heredity on our children. For marriage in the blood relatives and tell me about the precautions and treatment of heredity and also please tell %possibilities.

Hi sir, Please tell me about the effect of heredity on our children. For marriage in the blood relatives and tell me ...
Little higher chances of hereditory diseases among close relatives. No more specific answers can be given unless there is some disease detected in family.
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Hello sir, Please tell me treatment of DMD patients. The patients is 3 years old. Thank you.

Use syp Carnikid 5 ml twice a day. It's new remedy by astrum pharma for muscular dystrophies n delayed developmental problems.
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