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Mgu sconnection to MTHFR MUTATIONS
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This patient support community is for discussions relating to rare diseases and disorders. Some example include: Aarskog syndrome, Acoustic Neuroma, Angelman Syndrome, Behcet Syndrome, Bell’s Palsy, Canavan Disease, Carbon Baby Syndrome, Charcot Marie Tooth Disease, Chromosome Monosomy Disorders, Chromosome Trisomy Disorders, Devic's Disease, Dystonia, Ewing’s Sarcoma, Fragile X Syndrome, Immune Thrombocytopenia, Kawasaki Syndrome,Maple Syrup Urine Disease, Mastocytosis, McCune Albright syndrome, Pachygyria, Polycystic Kidney Disease, Prader-Willi Syndrome, Reiter’s Syndrome, Sickle cell anemia, Sturge-Weber syndrome, Trisomy Disorders, Usher Syndrome, Xanthinuria, Zollinger-Ellison syndrome.

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Mgu sconnection to MTHFR MUTATIONS

DOES MGUS HAVE ANY CONNECTION TO MTHFR DNA ANALYSIS RESULTS OF TWO IDENTIFIED MUTATIONS, C577T AND A1298C? IF ONE RECEIVES THE ABOVE MTHFR MUTATION RESULTS , SHOULD SHE TAKE THE TEST FOR THE M PROTEIN ASSOCIATED WITH  MULTIPLE MYALOMA?. Maternal Grandfather died of multiple myaloma  AGE 40 and mother is being monitored after diagnosis of mgus AT AGE 68. OVER THE YEARS, HER MOTHER HAS HAD NUMEROUS CHRONIC DISORDERS DIAGNOSEDWITH SYMTOMS (symptoms) INCREASING: IBS, CHRONIC FATIGUE, FIBROMYALGIA,ADHD, DEPRESSION, ANXIETY DISORDER AND BIPOLAR.  DAUGHTER HAS ENDOMETRIOSIS, 1 MISCARRIAGE AT AGE 38 AND 1 MALE CHILD AT AGE 40. AT AGE 46 SHE WAS DIAGNOSED WITH THYROIDITUS AND OVER THE YEARS TREATED FOR DEPRESSION PERODICALLY.
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selmaS
Allentown, PA