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Just found out my dd10 has positive factor 5 mutation. I think this may be one that comes in one and/or two copies but I don't know the specifics of her result. Her neurologist wants us to see a hemotologist soon. If anyone has experience with this, can you let me know your experience and what you have done as far as doctor's visits, lifestyle changes, etc? I don't know what might be necessary at age 10 with no signs of blood clots as opposed to later in life. She also has homozygous a1298c MTHFR gene mutation. We are currently waiting for her 23andme results. I don't want to go over board stressing about possible issues this fines and only focus on the big ticket items that will help her get well at this time. Thanks!
