Doctor insights on:
Alpha One Antitripsone
Father has hepatitis b his alpha feto protein increase from11767 to26434 iu/ml while taking medicines sorafenib200 , entacavir, daflon500, udiliv300 why?
S it fine to take glutathione 500mg,milk thistle extract 100mg, alpha lipoic acid 50mg, combined with d alpha tocopheryl acetate 400 iu?
Analysis: Why do you take all these items?. Where did you find such advice? Glutathione is a wonderful anti-oxidant, but does NOT cross into the brain, so of questionable value in bloodstream. Milk thistle extract has questionable benefit in most cases. Alpha lipoic useful in peripheral and central nerve disorders. You are far better off using mixed tocopherols, especially with gamma. See holistic doc ...Read more
Absolutely`: Very good but please remember that vitamins all work together in a team relationship so just taking one on its own may unbalance the team. ...Read more
S it fine to take glutathione 500mg,milk thistle extract 100mg, alpha lipoic acid 50mg, combined with d alpha tocopheryl acetate 400 iu and fish oil?
Not fine: Every single one of these is a waste of money. Some con-man is stealing your money. There is NO BENEFIT from any of them. ...Read more
Is vitamin E helpful for 8 months hb e beta thalassemia patient?Doctor prescribe her 200 iu vitamin E.Please advice
75y old(single kidney+chronic kidney disease),creatinine (~250),hemoglobin (~9.5),red cell count(3.6),Iron serum(107). Shall we use Aranesp (darbepoetin alfa) injection?
Not quite: Normal people have 4 Alpha globulin genes. Mutations in 1, 2, 3, or all 4 of the genes cause the 4 levels of Alpha thalassemia. One mutation = silent carrier (no symptoms), 2 mutat. = Alpha trait (mild anemia), 3 mutat. = HGB h disease (anemia sometimes needing transfusions), 4 mutat. = bart's disease (fatal before birth in almost all cases; lifelong transfusions needed to survive if born alive). ...Read moreSee 1 more doctor answer
CoQ 10 ALA: Yes. Thesexare safe together.Get a more detailed answer ›
Yes: Beta thalassemia disease is prevented if beta thal carriers do not have children with one another (if they have children together, some children will be normal, some carriers, and some have disease). The other, less desirable way, is to test fetuses during pregnancy and abort the fetuses who have beta thal major. ...Read moreSee 1 more doctor answer
Blood test: Sickle Beta cell Thalassemia is an inherited disorder and new born screening is available and should be done . This disorder is due to decreased synthesis or absence of beta globulin chains . It may manifest in infancy and early childhood and may cause serious medical problems which need to be treated ...Read moreSee 1 more doctor answer