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A reference range is usually defined as the set of values 95 percent of the normal population falls within (that is, 95% prediction interval). [2] It is determined by collecting data from vast numbers of laboratory tests. [citation needed]
The normal range of AFP for adults and children is variously reported as under 50, under 10, or under 5 ng/mL. [ 21 ] [ 22 ] At birth, normal infants have AFP levels four or more orders of magnitude above this normal range, that decreases to a normal range over the first year of life.
Infants were checked for clinical symptoms and laboratory signs of anemia 24 hours before and after the blood transfusion. The study found that groups 2 and 3 who had significant amount of blood loss, showed poor weight gain, pallor and distended abdomen. These reactions are the most frequent symptoms of anemia in very low birth weight infants. [8]
AFP is normally elevated in infants, and because teratoma is the single most common kind of tumor in infants, several studies have provided reference ranges for AFP in normal infants. [5] [6] [7] Perhaps the most useful is this equation: log Y = 7.397 - 2.622.log (X + 10), where X = age in days and Y = AFP level in nanograms per milliliter. [8]
The standard definition of a reference range for a particular measurement is defined as the interval between which 95% of values of a reference population fall into, in such a way that 2.5% of the time a value will be less than the lower limit of this interval, and 2.5% of the time it will be larger than the upper limit of this interval, whatever the distribution of these values.
Children: 50 to 120 μg/dL; TIBC: 240–450 μg/dL [1] Transferrin saturation: 20–50% [1] μg/dL = micrograms per deciliter. Laboratories often use different units and "normal" may vary by population and the lab techniques used; look at the individual laboratory reference values to interpret a specific test (for instance, your own).
It is essential to use age-specific normal reference values, as healthy infants and children usually have levels that would be considered elevated in adults. [4] Additionally, ALP levels are "not well defined" as of 2020, and can vary by sex and by racial group. [5]
Children with sickle-cell disease begin producing a defective form of hemoglobin called hemoglobin S instead, which form chains that cause red blood cells to change their shape from round to sickle-shaped. [35] These defective red blood cells have a much shorter life span than normal red blood cells (10–20 days compared to up to 120 days). [36]