study for the Genetics and Here9948/lessons/1533885/variants/1533885/take/5/Alert 1 of 1: Instructional Technology Subsidy Up..DISMISSC.karyotypediagram that shows how a trait isinherited in a familyd.carrierstructures of DNA and histonesthat form during cell divisione.amniocentesisprocedure used on a pregnantwoman to check the fetus for gef.pedigreenetic abnormalitiesg-nondisjunctionfailure of homologous chromo-somes to separate duringmeiosish.chromosomesall the DNA in a speciesinserting normal genes into cellswith mutant genes47°F Mostly cloudy or the Genetics and Here xssons/1533885/variants/1533885/take/5/1: Instructional Technology Subsidy Up.DISMISSorganism that has an allele for aa.gene therapytrait that is not expressedb.genomepicture of the pairs of chromo-somes in an organismC.karyotypediagram that shows how a trait isinherited in a familyd.carrierstructures of DNA and histonesthat form during cell divisionе.amniocentesisprocedure used on a pregnantwoman to check the fetus for ge-f. pedigreenetic abnormalitiesg.nondisjunctionfailure of homologous chromo-somes to separate duringmeiosish.chromosomes47°F Mostly cloudy

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organism that has an allele for a trait that is not expressed a. gene therapy b. genome picture of the pairs of chromo- somes in an organism C. karyotype diagram that shows how a trait is inherited in a family d. carrier structures of DNA and histones that form during cell division е. amniocentesis procedure used on a pregnant f. pedigree woman to check the fetus for ge- netic abnormalities g. nondisjunction failure of homologous chromo- somes to separate during meiosis h. chromosomes

organism that has an allele for a trait that is not expressed a. gene therapy b. genome picture of the pairs of chromo- somes in an organism C. karyotype diagram that shows how a trait is inherited in a family d. carrier structures of DNA and histones that form during cell division е. amniocentesis procedure used on a pregnant f. pedigree woman to check the fetus for ge- netic abnormalities g. nondisjunction failure of homologous chromo- somes to separate during meiosis h. chromosomes

3-2-1 Code It

6th Edition

ISBN:9781337660549

Author:GREEN

Publisher:GREEN

Chapter3: Icd-10-cm And Icd-10-pcs Coding Conventions

Section: Chapter Questions

Problem 1M

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Ten years into the future and you have just become a parent of a new born baby who apparently appears healthy. Will you subject your child to genetic testing? Support your answer in 3-4 sentences. only 3-4 sentences thank you.
Answer the following questions on Genetic Counseling: 1. What “soft” skills does a genetic counselor need that might not be quantified by achieving a degree in a STEM field. Soft skills are interpersonal skills like active listening, time-management, and problem solving. 2. Why are pedigrees a tool used in genetic counseling and what might they tell the person or people being counseled? 3. Identify two to three tricky ethical situations a genetic counselor may run into when working with a couple who are expecting a baby.
Give at least four different reasons for seeking genetic counseling.
Having all the necessary information about chromosomal abnormalities, complete the table below to assess your understanding of all the lessons included.
Distinguish between genetic screening programs for newborns and adults, and discuss the scope and implications of genetic counseling.
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Mike was referred for genetic counseling because he was concerned about his extensive family history of colon cancer. That family history was highly suggestive of hereditary nonpolyposis colon cancer (HNPCC). This predisposition is inherited as an autosomal dominant trait, and those who carry the mutant allele have a 75% chance of developing colon cancer by age 65. Mike was counseled about the inheritance of this condition, the associated cancers, and the possibility of genetic testing (on an affected family member). Mikes aunt elected to be tested for one of the genes that may be altered in this condition and discovered that she did have an altered MSH2 gene. Other family members are in the process of being tested for this mutation. Once a family member is tested for the mutant allele, is it hard for other family members to remain unaware of their own fate, even if they did not want this information? How could family dynamics help or hurt this situation?
Mike was referred for genetic counseling because he was concerned about his extensive family history of colon cancer. That family history was highly suggestive of hereditary nonpolyposis colon cancer (HNPCC). This predisposition is inherited as an autosomal dominant trait, and those who carry the mutant allele have a 75% chance of developing colon cancer by age 65. Mike was counseled about the inheritance of this condition, the associated cancers, and the possibility of genetic testing (on an affected family member). Mikes aunt elected to be tested for one of the genes that may be altered in this condition and discovered that she did have an altered MSH2 gene. Other family members are in the process of being tested for this mutation. Is colon cancer treatable? What are the common treatments, and how effective are they?
Mike was referred for genetic counseling because he was concerned about his extensive family history of colon cancer. That family history was highly suggestive of hereditary nonpolyposis colon cancer (HNPCC). This predisposition is inherited as an autosomal dominant trait, and those who carry the mutant allele have a 75% chance of developing colon cancer by age 65. Mike was counseled about the inheritance of this condition, the associated cancers, and the possibility of genetic testing (on an affected family member). Mikes aunt elected to be tested for one of the genes that may be altered in this condition and discovered that she did have an altered MSH2 gene. Other family members are in the process of being tested for this mutation. Seventy-five percent of people who carry the mutant allele will get colon cancer by age 65. This is an example of incomplete penetrance. What could cause this?
discusses the role of genetics in health status. Do you believe that genetic testing can be helpful in fighting disease? Would you consent or refuse genetic testing? Discuss your opinions in favor or against knowing your risks for developing disease. Post your answers under the topic-Genetic Testing Pro or Con?
Please Answer with reason: 3) The nurse is explaining the inheritance of Huntington disease (autosomal dominant) to a newly diagnosed patient whose partner does not have the gene mutation. Which statement should the nurse make regarding family planning? a. There is a 100% chance with each pregnancy that the child will inherit the gene for Huntington disease. c. There is a 50% chance with each pregnancy that the child will inherit the gene for Huntington disease b. There is a 25% chance with each pregnancy that the child will inherit the gene for Huntington disease d. There is a 0% chance with each pregnancy that the child will inherit the gene for Huntington disease.