Hereditary Angioedema Questions

Follow these herbal combination for complete cure
sootshekhar ras 1 tablet twice a day
ashta moorti avleh 10 gms twice a day
vyadhi har rasayan 125 mg twice a day.

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.

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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.

Give him kanchnaar guggulu regularly. But for proper diagnosis and prescription accordingly, you need to consult with his reports. Take care.

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.

Treatment of hydated cyst includes =
1.surgery
2. Removal of fluid from cyst
3. Medications
surgery removal of part of liver hepactectomy.

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

Hello lybrate-user. You need to consult a geneticist. Need to see all the x-rays and the child to consider further genetic testing. Thereafter only we will be able to advise regarding the course of the disease. All the best.