Qu'est-ce (qui) est ZC4H2 deficiency - définition
ZC4H2 deficiency
PROTEIN-CODING GENE LOCATED ON THE X-CHROMOSOME
User:Marielouisepaul/sandbox; Draft:ZC4H2 deficiency; Zinc finger C4H2-type; ZC4H2 deficiency; ZC4H2-Associated Rare Disorders (ZARD)
ZC4H2 (Zinc finger Cys4His2-type) is a protein-coding gene located on the X-chromosome. This gene encodes a protein which is a member of the so-called zinc finger domain-containing protein family.
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.
