Mitochondrial DNA Depletion Syndrome Questions

1. Avoid exposure to cold
2. Take bath with little warm water 3. Do steam inhalation regularly at least once a day
4. Warm salt water gargles daily 5 no cold water / cold drinks / ice creams and so on
6. No smoking/ avoid pollution 7. Wash hands after use of bath room and before and after eating food.
8 more warm liquids medicine can not be advised for open question for medicine contact on private consultation good luck.

Lipid myopathies (lm) are a group of muscular diseases with onset in all ages, due in most cases to enzymatic errors of lipid metabolism. Lm often, but not always, are characterized by lipid storage in muscle biopsy. Immunomodulatory/immunosuppressant drugs such as methotrexate, cyclosporine, tacrolimus, azathioprine, mycophenolate, rituximab and intravenous (ivig) or subcutaneous (subqig) immunoglobulin.
Corticosteroids such as prednisone or methylprednisolone.

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.

No it is not truth.
Blood group is not related to defects.
If you have faulty genes then it can cause defects.

Meet any post-graduate chest physician or geneticist and showing all records take the certificate that you have poland's syndrome.

If you are carrier or one copy of defective gene and your husband is also carrier or one copy of defective gene then your baby has chance of glutaric acidemia type 1.
if you husband is normal then baby will be normal

It is autosomal dominant meaning 50 % of children have chance to get same.
Evidence shows that the syndrome is associated with an increased risk of extraintestinal malignancy, especially carcinomas of the pancreas, breast, and reproductive organs.

Congenital deformities of spine are different and muscular dystrophies are different. They are not same.

It is a cancer of vocal cord.
But still in initial phase and outcome of the treatment can be favourable.

Hello lybrate-user. Treatment can be given only after seeing the reports. Depends whether it is biotinidase deficiency or something else
all the best.