<b>Kampo Treatment for Intractable Iron-Deficiency Anemia Due to Gastrointestinal Side Effects of Oral Iron S</b><b>upplement</b>
نویسندگان
چکیده
منابع مشابه
Anemia, Iron Deficiency, and Iron Deficiency Anemia
Anemia is one of the most widespread public health problems, especially in developing countries, and has important health and welfare, social, and economic consequences. These include impaired cognitive development, reduced physical work capacity, and in severe cases increased risk of mortality, particularly during the perinatal period. There is also evidence that anemia may result in reduced g...
متن کاملEffects of Nutritional variables in children with iron deficiency anemia
Introduction: Iron deficiency (ID) is the most prevalent nutritional disorder in the world. The prevalence of iron deficiency anemia (IDA) is about 9% in toddlers, 9-11% in adolescent girls and less than 1% in teenage boys. IDA presents when there is not sufficient iron for haemoglobin synthesis. In particular it has negative effects on the behavior, cognitive performance, immune system and phy...
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Background: Postpartum anemia can develop after delivery because of unforeseen medical problems during and after delivery which could complicate a mother’s ability to properly care for her newborn child. The current treatment for postpartum anemia is oral iron supplementation but this treatment has been associated with several gastrointestinal side effects. Alternative treatments include blood ...
متن کامل55 Cases of Iron Deficiency Anemia
55 cases of iron SUMMARY deficiency anemia were hosThis pitalized type at of anemia Bahrami was Hospital found in to be one the year. most Our frequent study cause showed of that anemia in in infants infants, in malnutriIran. tion older· was age the other main causes cause such of as anemia, GI while leeding,in ethiologie parasitosis of and the chronic disease. Most infection infants were wit...
متن کاملIron refractory iron deficiency anemia.
Iron refractory iron deficiency anemia is a hereditary recessive anemia due to a defect in the TMPRSS6 gene encoding Matriptase-2. This protein is a transmembrane serine protease that plays an essential role in down-regulating hepcidin, the key regulator of iron homeostasis. Hallmarks of this disease are microcytic hypochromic anemia, low transferrin saturation and normal/high serum hepcidin va...
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ژورنال
عنوان ژورنال: Kampo Medicine
سال: 2018
ISSN: 0287-4857,1882-756X
DOI: 10.3937/kampomed.69.48