2. INTRODUCTION Counseling is a process of communicating between two or more persons who meet to solve a problem, resource a curse or take decision on various matters. It is not a one way process where in the counseling tells the client what to do nor it is a forum for presentation of the counselor’s values. Genetic counseling process follows these basic characteristic of a counseling process. It is undertaken with families confronted with genetic and inherited disorders. Sheldon Reed proposed the terminology “GENETIC COUNSELING in 1947”.
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5. Reassure people who are concerned that their child may inherit a particular disorder that the disorder will not occur.
6. Allow people who are affected by inherited disease to make informed choice about future reproduction.
9. An amniocentesis yields n unexpected results (such as chromosomal defect in the unborn baby).
10. Either parent or close relative has an in heritance disease or birth defect, either parents already has children with birth defect or genetic disorders.
11. The mother has had two or more miscarriage or a baby dies in infancy.
14. Pedigree Charting At a glance this offers in a concise manner the state of disorder in a family. Constructing a pedigree with proper interrogation though time consuming, is ultimately rewarding. If forms an indispensable step towards counseling Estimation of Risk: It forms one of the most important aspect of genetic counseling. It is often called recurrence risk. To estimate it one requires to take into account following points: Mode of inheritance Analysis of pedigree or family tree Results of various tests
21. Above all, communication skills to transmit facts in an effective manner i.e. making them more acceptable and palatable.
22. Management: In genetics, “Treatment” implies a very limited scope. It naturally aims for prevention rather then cure. In fact for most of the genetic disorders cure is unknown. Treatment is therefore directed towards minimizing the damage by early detection and preventing further irreversible damage. For example n PKU, i.e. phenylketonuria. This disorder is characterized by a deficiency of phenylalanine hydroxylase enzyme, which is necessary for the conversion of phenylalanine to tyrosine
23. APPLICATIONS OF GENETIC COUNSELING Genetic counselors work with people concerned about the risk of an inherited disease or condition. These people represent several different populations
24. Prenatal Genetic Counseling There are several different reasons a person or couple may seek prenatal genetic counseling. If a woman is of age 35 or older and pregnant, then there is an increased chance that her fetus may have a change in the number of chromosomes present. Changes in chromosome number may lead to mental retardation and birth defects
25. Prenatal tests that are offered during genetic counseling include Level II Ultrasound The maternal serum AFP Chorionic Villus sampling (CVS) Amniocentesis
26. Pediatric Genetic Counseling Families or pediatricians seek genetic counseling when a child has features of an inherited condition. Any child who is born with more than one defect, mental retardation or dysmorphic features has an increased chance of having a genetic syndrome. A common type of mental retardation in males for which genetic testing is available is fragile X-syndrome.
27. Adult Genetic Counseling Adults may seek genetic counseling when a person in the family decided to be tested for the presence of a known genetic condition, when an adult begins exhibiting symptoms of an inherited condition, or when there is a new diagnosis of someone with an adult-onset disorder in the family In addition, the birth of a child with obvious features of a genetic disease leads to diagnosis of a parent who is more mildly affected Genetic counseling for adults may lead to the consideration of presymptomatic genetic testing
28. Cancer Genetic Counseling A family history of early onset breast, ovarian or colon cancer in multiple generations of family is a common reason a person would seek a genetic counselor who works with people who have cancer. While most cancer is not inherited, there are some families in which a dominant gene is present and causing the disease A genetic counselor is able to discuss the chances that the cancer in the family is related to a dominantly inherited gene. The counselor can also discuss the option of testing for the breast and ovarian cancer genes
29. ROLE OF A NURSE IN GENETIC COUNSELING Guiding a women or couple through prenatal diagnosis. Helping parents make decision in regard to abnormal prenatal diagnostic results. Assisting parents who have had a child with a birth defect to locate needed service and support. Providing support to help the family deal with the emotional impact of a birth defect. Coordinative services of other professionals, such as social workers, physical and occupational therapist, psychologist & dietician.
30. CONCLUSION Genetic Counseling enables couples / affected individual to make decision about a future pregnancy. It helps the affected individual to educate and cope with the disorders with minimal clinical problem. Therefore Genetic Counseling is done in an objective manner, so that any treatment selected remains the personal choice of the individual involved. Hence thorough knowledge of the disease for giving information regarding the cause and risk factors of the disease is necessary before counseling.
31. BIBLIOGRAPHY Keya Lahiri “Clinical genetics” 1ST edition 2005, Jaypee Publications, page no: 41, 104-106. Suresh kumarSharma,”Human genetics in nursing” 1st edition 2007, Jaypee Publication, page no: 106-109. Trulamayer, “Foundation of maternal newborn nursing” Saunder Publication, page no : 81-84. Ladewig, “Maternal newborn nursing”5th edition, Benjamin Publication Company, page no: 167-175 . Elizabeth M. Variorolis ”Foundation of psychiatrics mental health nursing” 4th edition 2002, Saunders Publication, page no:210-211. http://www.medindia.net/patient/patient info/genetic counseling http://www.kidshealth.org/pregnancy/newborn/medical problems/genetic counseling.html