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1,974 Possible Causes for Folic Acid Decreased, Hemoglobin Decreased, Thyroxin Binding Globulin Increased

  • Third Trimester Pregnancy

    The concomitant phenomenon of a third trimester pregnancy with a significant degree of pelvic organ prolapse is extremely rare. We report on a patient with pelvic organ prolapse complicating third trimester pregnancy treated by concomitant cesarean hysterectomy and abdominal sacrocolpopexy. A 30-year-old woman,[…][]

  • Inflammatory Bowel Disease Type 1

    Doctors prescribe folic acid to decrease the side effects of methotrexate. Cyclosporine is given by injection in high doses.[] Folic acid can reduce the risk of liver toxicity. Infliximab has been linked to acute liver injury in addition to reactivation of hepatitis B. C.[] The effect is dose related and it is unaffected by supplemental folic acid. 172– 177 11.3 Influence of disease activity on the course and outcome of pregnancy ECCO Statement[]

  • Myxedema

    Macroglossia is classified as true macroglossia, which exhibits abnormal histology with clinical findings, and relative macroglossia, in which normal histology does not correlate with pathologic enlargement. This report describes an atypical case of morbidity with massive macroglossia secondary to myxedema; the[…][]

  • Ectopic Pregnancy

    acid antagonist antidote, up to four doses of each until the β-hCG level decreases by 15% on two consecutive days [ 8 ].[] The multidose regimen alternates an every other day dose of intramuscular MTX 1.0 mg/kg with an every other day dose of intramuscular leucovorin calcium 0.1 mg/kg, a folic[]

  • Ulcerative Colitis

    Successive courses showed decreased efficacy and increased CS-dependence, limiting CS-treatment.[] An older age at diagnosis, longer interval from diagnosis to CS-therapy, lower CRP and higher hemoglobin predicted better prognosis.[] Logistic regression analysis gave a predictive response mainly due to the age at diagnosis, the interval from diagnosis to CS-therapy, and C-reactive protein (CRP) or hemoglobin[]

  • Hereditary Spherocytosis

    All experienced an increase in hemoglobin and decrease in reticulocyte count early after LPS and at last follow-up. Twenty-two were sent for genetic analysis.[] […] bone marrow compensation Need for continuous tranfusions decreases to 30% after first year of life Splenectomy Decision to proceed with splenectomy must take into account[] The hemoglobin levels increased by 1 g/dl, mean corpuscular hemoglobin concentration decreased by 1 g/dl, and the reticulocyte count decreased by 0.93%.[]

    Missing: Thyroxin Binding Globulin Increased
  • Celiac Disease

    There is a progressive decrease in the titer of celiac related antibodies.[] Patients should also be evaluated for osteoporosis, thyroid dysfunction, and deficiencies in folic acid, vitamin B12, fat-soluble vitamins, and iron, and treated appropriately[] This may lead to deficiencies in vitamins (such as folic acid) and minerals (e.g. iron and calcium).[]

    Missing: Thyroxin Binding Globulin Increased
  • Folate-Deficiency Anemia

    Anemia is caused due to the decrease of a compound called hemoglobin in the blood.[] Folic acid might decrease the effectiveness of pyrimethamine (Daraprim) for treating parasite infections. Dosing considerations for Folic Acid.[] Anemia is a condition that results from either a decrease in the size or number of red blood cells, or in the amount of hemoglobin, which is the red pigment in red blood cells[]

    Missing: Thyroxin Binding Globulin Increased
  • Autoimmune Hemolytic Anemia

    Laboratory data revealed progressive decrease in hemoglobin during her hospitalization due to pulmonary infection in 2016.[] Some of these include: Vitamin B12 level —blood level may be low when deficient in B12 Folic acid level —blood level may be low if deficient in this B vitamin Methylmalonic[] He presented with a markedly elevated C-reactive protein (CRP; 46 mg/L [normal, 0-5 mg/L]) before onset of a decrease in hemoglobin.[]

    Missing: Thyroxin Binding Globulin Increased
  • Cystic Fibrosis

    […] and development while decreasing or eliminating transfusional iron overload, which is the leading life-threatening factor in patients with this disease.[ 134 ] Butyrate analogs[] The development of an effective therapy to increase hemoglobin levels in homozygous β-thalassemia, without the use of red blood cell transfusions, could allow normal growth[] […] are able to induce erythroid differentiation[ 135 – 137 ] and stimulate hemoglobin F production in human erythroid progenitors in vitro .[ 138 – 140 ] In vivo, they reactivate[]

    Missing: Thyroxin Binding Globulin Increased

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