P14 deficiency - definitie. Wat is P14 deficiency
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Wat (wie) is P14 deficiency - definitie


P14 deficiency         
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MEDICAL CONDITION
User:Uaaugauagaug/sandbox
P14 deficiency is a rare autosomal recessive disease characterized as a primary immunodeficiency syndrome. This disease was first identified within a white Mennonite family by Professor Bodo Grimbacher and Professor Christoph Klein’s teams in 2006.
Fluorine deficiency         
MEDICAL CONDITION
Fluorine Deficiency; Fluoride deficiency
Fluoride or fluorine deficiency is a disorder which may cause increased dental caries (or tooth decay, is the breakdown of dental tissues by the acidic products released by the "bacterial fermentation of dietary carbohydrates.") and possibly osteoporosis (a bone disorder which leads to a decrease in bone mass, and an increase in bone fragility), due to a lack of fluoride in the diet.
Pseudocholinesterase deficiency         
MEDICAL CONDITION
Plasma cholinesterase deficiency; Vysya enzyme deficiency
Pseudocholinesterase deficiency is an autosomal recessive inherited blood plasma enzyme abnormality in which the body's production of butyrylcholinesterase (BCHE; pseudocholinesterase aka PCE) is impaired. People who have this abnormality may be sensitive to certain anesthetic drugs, including the muscle relaxants succinylcholine and mivacurium as well as other ester local anesthetics.