РефератыИностранный языкCYCYSTIC FIBROSIS Essay Research Paper CYSTIC FIBROSISONE

CYSTIC FIBROSIS Essay Research Paper CYSTIC FIBROSISONE

CYSTIC FIBROSIS Essay, Research Paper


CYSTIC FIBROSIS


ONE OUT OF EVERY 2,500 BIRTHS IN THE UNITED STATES WILL BE DIAGNOSED


WITH CYSTIC FIBROSIS. THIS FACT MAKES CYSTIC FIBROSIS ONE OF THE MOST COMMON


GENETIC DISEASES IN THE NATION. ABOUT 30,000 AMERICANS HAVE THE DISEASE, BUT


EVEN THOUGH CYSTIC FIBROSIS IS THE NATIONS MOST COMMON GENETIC DISEASE THE


MAJORITY OF AMERICANS KNOW LITTLE ABOUT IT. CYSTIC FIBROSIS IS RELATIVELY


COMMON IN CALCASTION PEOPLE BUT RARE IN AFRICAN-AMERICAN. THE DISEASE IS VERY


UNCOMMON IN MONGOLIANS. FIVE PERCENT OF THE POPULATION IN THE UNITED STATES ARE


CARRIERS OF THE GENETIC DISEASE.


CYSTIC FIBROSIS, SOMETIMES CLASSIFIED AS MUCOVISCIDOSIS, IS A DISORDER


IN WHICH THE EXCRORINE GLANDS SECRETE ABNORMALLY THICK MUCUS. THIS LEADS TO THE


OBSTRUCTION OF THE PANCREAS AND CHRONIC INFECTIONS OF THE LUNGS, WHICH GENERALLY


CAUSES DEATH IN CHILDHOOD OR EARLY ADULTHOOD. SOME MILDLY AFFECTED PATIENTS MAY


SURVIVE LONGER. PATIENTS WITH PANCREATIC INSUFFICIENCY TAKE PANCREATIC ENZYMES


WITH MEALS. THOSE WITH RESPIRATORY INFECTIONS ARE TREATED WITH ANTIBIOTICS,


MOSTLY WITH AEROSOLS THAT RELIEVE CONSTRICTION OF THE AIRWAYS. PHYSICAL THERAPY


IS USED TO HELP PATIENTS COUGH UP THE OBSTRUCTING MUCUS. INTESTINAL OBSTRUCTION,


WHICH OCCURS MOSTLY IN INFANCY, MAY REQUIRE SURGERY.


IN 1989, RESEARCHERS FOND THE ABNORMAL GENE THAT CAUSES CYSTIC FIBROSIS.


THIS GENE IS LOCATED ON CHROMOSOME 7 . A PERSON WHO HAS TWO CYSTIC FIBROSIS


GENES HAS THE DISEASE . A PERSON THAT CARRIES ONE OF THE GENES DOES NOT HAVE THE


GENETIC DISEASE, BUT IS A CARRIER.


THE SYMPTO

MS OF CYSTIC FIBROSIS SOMETIMES OCCUR IMMEDIATELY AFTER BIRTH.


MUCUS SECRETIONS MAY APPEAR IN THE BABY?S INTESTINES, WHICH CAN CAUSE


OBSTRUCTION IN THE INTESTINES. IN ALL CASES, THE CHILD WILL GAIN LITTLE WEIGHT


RIGHT FROM BIRTH, BECAUSE THE PANCREAS IS NOT PRODUCING ENZYMES. LITTLE TO NO


NUTRIENTS ARE ABSORBED IN THE CHILD?S SYSTEM. A CHILD WITH CYSTIC FIBROSIS MAY


HAVE REOCCURRING RESPIRATORY INFECTIONS, ALONG WITH COUGH AND FEVER. THIS MAY BE


MORE SEVERE AND PERSISTENT THAT NORMAL THIS IS A RESULT OF THE THICK, STICKY


MUCUS THAT WILL HOLD AND TRAP GERMS IN THE BRONCHIAL TUBES. IT SHOULD BE TAKEN


IN TO CONSIDERATION THAT CHILDREN WITH CYSTIC FIBROSIS HAVE LARGE APPETITES AND


EAT A GREAT DEAL. IN SPITE OF THEIR MALNUTRITION, THEY ART NOT IN PAIN AND DO


NOT GENERALLY FEEL IT.


EXTRACTS OF ANIMAL PANCREAS, IN POWDER OR GRANULE FORM, ARE PRESCRIBED


TO REPLACE THE MISSING ENZYMES FROM THE PANCREAS, AND THE AMOUNT OF FAT IS


DECREASED IN THE CHILD?S DIET. WITH THIS TREATMENT THE CHILD BEGINS TO GAIN


WEIGHT. TO KEEP THE LUNGS FREE OF AS MUCH MUCUS AS POSSIBLE , THE PATIENTS MAY


NEED TO HAVE DAILY RESPIRATORY PHYSICAL THERAPY. ANY RESPIRATORY INFECTION THAT


ARISE ARE TREATED WITH LARGE AMOUNTS OF ANTIBIOTICS.


CYSTIC FIBROSIS CAN NOT YET BE CURED. ALTHOUGH THE IDENTIFICATION OF


CHROMOSOME 7 HAS PAVED THE WAY FOR GENE THERAPY. ANTIBIOTICS AND ENZYMES ARE NOT


THE ONLY TREATMENTS FOR CYSTIC FIBROSIS. ONE RELATIVELY NEW TREATMENT IS A


BIOTECH DRUG THAT THINS THE MUCUS, WHICH HELPS THE LUNGS FUNCTION BETTER AND


REDUCES THE RISK OF INFECTIONS. GENE THERAPY IS STILL IN EXPERIMENTAL STAGES.

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