Member Comments are provided by individuals and reflect their personal opinions only. Under NO circumstances should you act on any advice or opinion posted in this forum.  ALWAYS check with your personal physician before taking any action regarding your health! MedHelp International and our partners, sponsors and affiliates have no obligation to monitor any comments posted on this site, or the content and/or accuracy of such exchanges. MedHelp International does not endorse the views of any user.
Genetics  (Expert Forum)
 | 
MTHFR QUESTIONS
Answered by
AccessDNA
Welcome to the Genetics Forum! Questions in the Genetics Forum are being answered by genetic experts from AccessDNA. This forum is for questions and support regarding a person’s predisposition to a variety of medical conditions such as Ashkenazi Jewish Diseases, Bleeding Disorders, Blood Clotting Disorders, Cancer Genetics and Hereditary Cancer Syndromes, Chromosome Abnormalities, Congenital Birth Defects, Cystic Fibrosis, Family History, Fragile X Syndrome, Infertility, Newborn Screening, Rare Genetic Disorders, Prenatal Screening and Testing. This forum is for questions and support regarding a person’s predisposition to a variety of medical conditions such as Alzheimer’s Disease, Blood-clotting Disorders, Breast Cancer, Cystic Fibrosis, Diabetes, Marfan Syndrome, Ehlers-Danlos Syndrome, etc.

MTHFR QUESTIONS

by stargazerm43, Jul 30, 2009 06:19PM
Could my granddaughters diagnosis of MTHFR come down thru the family due to my fathers rare blood disease of Waldenstromacroglobulanmeia? I don't know what type of mthfr she has. What natural  supplements and vitamins can we use for her?

by Jordanna Joaquina, MS, CGC, Aug 04, 2009 01:18PM
To: stargazerm43
Waldenstrom macroglobulinemia (WM) is a rare subtype of non-Hodgkin lymphoma. The exact cause of WM is not known. However, researchers believe that genetics may play a role in WM in some cases, because the disease has been seen to run in families. A few genes and genetic regions have been implicated in some familial cases of the disease, but additional genes are also likely to be involved.

MTFHR is separate and is caused by variations in the MTHFR gene. This gene is important in the metabolism of an amino acid called homocysteine. Variants in the gene are inherited.

When a person has two variants, they inherited one variant from their mother and the other variant from their father. When a person has one variant, they inherited the variant from either their mother or their father.

The clinical treatment for women with MTHFR variants who are trying to get pregnant or who are pregnant is not well established and is often debated. The one universally accepted recommendation is to take folic acid supplements (amount to be discussed with her doctor). Depending on a person’s medical and pregnancy history, other treatments may be suggested as well.

We recommend that your granddaughter meet with a genetic counselor who can review her pregnancy and family history. A genetic counselor can be found through the National Society of Genetic Counselors website or through companies like mine, AccessDNA.
Member Comments (2)

by stargazerm43, Jul 30, 2009 06:23PM
To: mthfr questions
Forgot to add that my granddaughter has mis/car. 2 times , twins both times, one set fraternal one set identical.
Continue discussion
RSS Expert Activity
What You Don't Know About Breathing...
Nov 24 by Steven Y Park, MD
Thanksgiving
Nov 23 by Thomas Dock, Vet. Technician
Snoring As Your Internal Smoke Alar...
Nov 22 by Steven Y Park, MD