Doctor insights on:
Wound Healing With Thalassaemia Trait
Had a simple vulvectomy 5 wks ago-area of over-granulation tissue removed-no VIN. Wound healing well altho 1 stitch opened. Still have pain- normal?
Wound healing is a field of study in which a person looks at factors that helps wounds heal and factors that are harmful to wounds trying to heal, in order to find the best treatment for each wound. Wounds can be from infections, surgeries, accidents, etc... Poorly healing wounds can occur where there is inadequate blood circulation, such ...Read more
My partner is consistent with haemoglobin e-trait. I have normal hb chromatographic pattern. Is there any chance of thalassaemia of our new born baby?
Electrophoresis, but: Levels of hemoglobin h and hemoglobin barts should make the distinction straightforward though there may be modifying genes that could make interpretation. The real question is the implications in planning your family and for this perhaps you would like to have genetic testing done. Any hematologist would probably enjoy helping you out. Good luck. ...Read more
It is what it is ...: Thalassemia is a number of inborn (genetic) disorders of hemoglobin (check out http://www.Mayoclinic.Com/health/thalassemia/ds00905 & http://www.Nhlbi.Nih.Gov/health/health-topics/topics/thalassemia/). Carries have just one gene while those w/full blown disorder have both. As a carrier, there're few clinical symptoms so it's "safe" for you, not that you could do anything about it! ...Read more
Thalassemias: Both α and β thalassemias are often inherited in an autosomal recessive fashion, although this is not always the case. Cases of dominantly inherited α and β thalassemias have been reported, the first of which was in an irish family with two deletions of 4 and 11 BP in exon 3 interrupted by an insertion of 5 BP in the β-globin gene. For the autosomal recessive forms both parents must be carriers. ...Read more
Can be: This is an inherited disease, commonly found in people with mediterranean ancestors. The body makes an abnormal amount of hemoglobin. You must be mindful of the higher risk of anemia due to the destruction of red blood cells. See your md for evaluation, treatment as needed, and monitoring. ...Read more
My grandfather a htn and CKD patient with dm and a thalassaemia carrier has just started dialysis at the age of 81 what are his chances of survival?
Time on dialysis: That is a difficult question to answer. You should ask his neprhologist for his opinion about your father's survival. The literature shows that 50% of patients starting dialysis over 75 years of age die within 2 years and the mean survival of that cohort is 31 months. A healthy male in the us has a life expectancy of 7.4 years at age 81. These data are for your information only. ...Read moreSee 1 more doctor answer
My daughter is a beta thalassaemia major patient & taking regular blood transfusion for 10 yrs. Now she has hep c type 4 &viral load is 133964. Cure?
Don't rush: Young people tend to have fairly slow progression of liver damage wit hepatitis c. The pace of new drug development over the next 5-10 years will transform this disease. Get informed. Follow sophisticated websites like natap.Org for the latest clinical trial data. Today, treatment of hcv in people like your child is complicated, but we will have easier to tolerate regimens in genotype 4 in 2-4 y. ...Read moreSee 1 more doctor answer
Complicated process: Multiple factors involved. White blood cells and platelets travel to the site for immune system and blood clotting. Collagen fibers heal across, and new blood vessels grow in. Collagen fibers remodel. Proper body protein level and appropriate vitamin levels help with healing. Poor nutrition, diabetes, cigarette smoking, infection, poor blood supply, Prednisone can delay or prevent proper healing. ...Read moreSee 1 more doctor answer
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