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Treatment consists of dietary adjustment (low fat—high calorie) and
administration of vitamins, pancreatin, and antibiotics to ward off secondary infections. Special measures are necessary to decrease
viscosity of pulmonary secretions; aerosol application of recombinant human dbase, an enzyme that digests
sticky extra cellular DNA that helps form these viscous secretions, was approved in 1993. In some cases lung transplantation is helpful. The identification of
abnormal gene (1989) paved
way for gene therapy aimed at altering
genetic structure by transferring to
patient cells with normal genes.
Identification of
genes has also made tests for genetic screening and diagnosis possible. Evolutionary biologists have suggested that
gene that must be inherited from both parents to cause
disorder, affords carriers some protection against cholera, a disease that kills through profound loss of fluids.
Health is wealth they say. Monitoring our health should be our primary concern. Staying away from any infections by living a healthy life is
best solution to fight SINUS CYSTIC FIBROSIS INFECTION!
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