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Genetic Counselor Awareness PowerPoint Presentation

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Description : Check out this medical PowerPoint presentation titled "Genetic Counselor Awareness-from arrays to sequencing”.

This medical PowerPoint presentation is about Genetic Counselor, Genetic Counseling and Careers in Genetic Counseling.

A genetic counselor is a healthcare professional who specializes in the field of genetics and provides information and support to individuals and families who may be at risk for or affected by genetic conditions. They work with individuals to assess their risk of developing certain genetic conditions or passing them on to their children, and help them make informed decisions about genetic testing, family planning, and medical management.

Genetic counselors often work in a variety of settings including hospitals, clinics, research facilities, and private practice. They may work with individuals of all ages, from newborns to adults, and may specialize in areas such as prenatal genetics, cancer genetics, cardiovascular genetics, and pediatric genetics.

In addition to providing counseling services, genetic counselors also play an important role in research, education, and advocacy related to genetics and genetic conditions. They work to raise awareness about genetic conditions, promote genetic literacy, and advocate for policies that ensure equitable access to genetic testing and counseling services.

Tags : Genetic Counselor, Genetic Counseling, Careers in Genetic Counseling, Medical Genetics, Medical Genetics PowerPoint presentation

Published on : Jun 07, 2023 | Views : 792 | Downloads : 0

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What is a Genetic Counselor?
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Genetic counselors are specialists who provide personalized care for your genetic health.
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What is a Genetic Counselor?
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Genetic counselors work in a variety of settings.
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The largest specialty areas for genetic counselors are cancer, prenatal and pediatric genetics, but genetic counselors are an important part of the healthcare team, working in a variety of specialties. Specialty Areas
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What do genetic counselors do? Help you understand your genetic risks based on your family history Work with you to develop a personalized medical plan Enable you to make an informed decision about genetic testing Explain results and help you process the medical and and emotional implications of genetic testing Connect you to resources, support groups, or other patients
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Some Reasons to See a Genetic Counselor You are pregnant or considering pregnancy and have questions about your genetic risks to the baby You, your child or a family member has been diagnosed with a genetic condition, or there is concern for a genetic condition You, your child or a family member have unexplained medical concerns that could be due to genetic causes
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Common Diseases that May Have a Genetic Component Cancer Heart disease Diabetes Stroke Alzheimer's
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Preparing for your visit with a Genetic Counselor Family health history Medical records Results of any genetic tests A list of your questions and concerns
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What happens during a genetic counseling appointment? Genetic counselors ask about your family health history and discuss any genetic risks to you and your family members Offer continued support through the testing and results process Talk about any appropriate options in terms of genetic testing and medical management Help you understand available tests and possible results, and help you decide when and if to pursue genetic testing
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How much does genetic counseling cost? Health insurance typically pays for genetic counseling and in many cases pays for genetic testing when it is recommended by a doctor Check with your insurance company to verify coverage
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Explore a Career as a Genetic Counselor
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There are so many reasons to becomea Genetic Counselor.
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Genetic Counselor was named one of the “25 Amazing Healthcare Support Jobs” and one of the “100 Best Jobs” in 2020 - U.S. News and World Report
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By the Numbers… Employment of genetic counselors is projected to grow 29% through 2026. Average growth is 7%. -Bureau of Labor Statistics The average salary for a full-time genetic counselor in 2019 was $94,900 and ranges up to $224,000 depending on specialty area and experience. – NSGC 2020 Professional Status Survey More than 87% of graduating GCs in 2016 and 2017 had accepted a position before graduation. - NSGC 2020 Professional Status Survey 92% of genetic counselors report they are satisfied with their job. – NSGC 2020 Professional Status Survey
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The Education Path A bachelor’s degree, typically in: biology social science or a related field A master’s degree in genetic counseling from an accredited program: coursework clinical training research ABGC and/or CAGC-ACCG Certification (USA & Canada) after passing the Board Examination. Many states also require licensure to practice.
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Genetic Counseling Program Coursework Human genetics Embryology Ethics Counseling techniques Genetic testing technology
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Interested in Applying to a Genetic Counseling Program? For tips and information, visit the Association of Genetic Counseling Program Directors https://agcpd.org/AdmissionsInfo
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A Range of Career Possibilities Working with patients Laboratories Research Academia Industry Professional and patient organizations Healthcare administration Public health Policy
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Any role you can imagine and create for yourself A Range of Career Possibilities
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When and Why Should I Refer to a Genetic Counselor?
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Why work with a Genetic Counselor? Increase patient satisfaction Make informed decisions Save time and money
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Prenatal Indications for Genetic Counseling Mother will be 35 years or older at time of delivery (singleton) Mother will be 33 years or older at time of delivery (twins) Consanguineous union Abnormal first or second trimester maternal screening Exposure to known or potential teratogen Fetal anomaly/anomalies Positive carrier screen for genetic condition Personal history of stillbirths, previous child with hydrops or SIDS, recurrent pregnancy losses Either partner with a family history of birth defects, chromosomal anomalies, potentially genetic hearing/vision loss, intellectual disability or autism
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Oncological (Cancer) Indications for Genetic Counseling Personal or family history of cancer(s) known to be associated with a hereditary condition, such as: Breast Ovarian Colorectal Uterine Pancreatic Gastric Neuroendocrine Metastatic prostate cancer This should be considered in the context of: A compelling family history Young age at onset Bilateral or second primary cancers And/or familial clustering of related tumors Childhood onset cancer
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Abnormal newborn screening results Child of a parent with a known chromosomal abnormality or rearrangement (balanced or unbalanced) A single major, or multiple major and/or minor anomalies Dysmorphic features Hypotonia or hypertonia Failure to thrive A known metabolic disorder or symptoms of a metabolic disorder (e.g., intractable seizures, hepatosplenomegaly, acidosis, cyclic vomiting, persistent hypoglycemia, developmental regression, and unusual body odor) Abnormal brain MRI findings (e.g., leukodystrophy, periventricular calcifications, unidentified bright objects, or a malformation) Pediatric Indications for Genetic Counseling - Newborn/Infant
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Autism or pervasive developmental disorder Unusual behaviors, especially when associated with minor malformations and developmental delay Unexplained intellectual disability or global developmental disorder An unusual growth pattern such as overgrowth, short stature, or hemihypertrophy Evidence of a connective tissue disorder (e.g., extreme joint laxity, poor wound healing, or a marfanoid habitus) Congenital eye defects or blindness associated with problems (e.g., microphthalmia, cataracts, megalocornea, retinitis pigmentosa, or cone-rod dystrophy) Pediatric Indications for Genetic Counseling - Childhood
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Pediatric/Adult Indications for Genetic Counseling A recognized or suspected genetic syndrome, including a chromosomal or single gene disorder A significant family history of medical or psychiatric conditions Unusual skin findings (e.g., multiple types of lesions, multiple lipomas, numerous hypo or hyperpigmented lesions, and albinism) Problems with clotting, including disorders such as hemophilia and thrombophilia
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Pediatric/Adult Indications for Genetic Counseling Progressive muscle weakness that might be associated with a genetic disorder (e.g., a form of muscular dystrophy, spinal muscular atrophy, or myotonic dystrophy) Other neurologic condition that might be associated with a genetic predisposition (e.g., peripheral neuropathy, unexplained myopathy, progressive ataxia, or any progressive neurologic disorder without a clear, nongenetic cause) An immunodeficiency or significant immune problem Cardiomyopathy not secondary to a viral infection
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Case Studies
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Family History Pedigree: also called a “family tree”; a tool genetic counselors use to visualize a family health history and identify recognizable patterns Pedigree created using http://www.progenygenetics.com/online-pedigree/
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Cancer Genetics
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Meet Mary 45-year-old woman recently diagnosed with breast cancer Family history of cancer, including a mother with ovarian cancer who passed away at 70 Especially concerned about risks for her daughters (ages 22 and 25)
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Mary’s Family History
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Hereditary Breast Cancers Around 10-15% of all breast cancers are hereditary People with alterations in the genes BRCA1 or BRCA2 have greatly elevated chances to develop certain cancers, especially female breast (up to 85% risk) and ovarian (up to 45% risk) Other features may include: Multiple affected individuals Younger age of onset Affected individuals may have: bilateral breast cancer and/or triple negative breast cancer multiple primary cancers which may include breast, ovarian, male breast, pancreatic, prostate, or melanoma cancers
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In Mary’s Case She elected to undergo genetic testing A BRCA1 pathogenic variant was identified, confirming a diagnosis of hereditary breast and ovarian cancer syndrome (HBOC) Changed Mary’s medical management, including more screening and options for surgery and medications to reduce risks Allowed for testing of at-risk family members and early intervention in those with the same pathogenic variant
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Meet Joe 55-year-old male recently diagnosed with colon cancer Family history of cancer, including a mother with uterine cancer who passed away at 50, a sister who had precancerous colon polyps, and a maternal uncle who had colon cancer at age 47 Especially concerned about risks for his daughters (ages 27 and 31)
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Joe’s Family History
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Hereditary Colorectal Cancers Around 10% of all colorectal cancers are hereditary Of those, the majority are due to Lynch syndrome caused by alterations in the MLH1, MSH2, MSH6, PMS2, or EPCAM genes. People with Lynch syndrome have greatly elevated chances to develop certain cancers, especially colorectal, uterine, ovarian, gastric, and a few others Other features may include: Younger age of onset Precancerous colon polyps Individuals at high risk for colon cancer can significantly decrease this risk by having more frequent colonoscopies, beginning at a younger age
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In Joe’s Case Joe elected to undergo genetic testing An alteration in MSH2 was identified, confirming a diagnosis of Lynch syndrome Changed Joe’s medical management, including more screening and options for surgery Allowed for testing for at-risk family members and early intervention in those who also inherited the MSH2 alteration
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Pediatric Genetics
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In Pediatric Genetics 4-year-old boy, David, comes to clinic due to short stature, developmental delay and an insatiable appetite Parents remark that he was very “floppy” as a baby The geneticist and genetic counselor immediately suspect a diagnosis, and counsel the family about testing options
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Prader-Willi Syndrome Rare genetic condition affecting ~1/30,000 people Majority of cases are sporadic Recommended treatment includes growth hormone therapy Very specific genetic testing indicated, which may not be understood by a healthcare practitioner outside of genetics Parents elect testing, which returns positive and David is diagnosed with Prader-Willi syndrome
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Prenatal Genetics
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Meet Ann 39-year-old woman, 13 weeks pregnant Ann underwent noninvasive cell-free DNA prenatal screening (NIPS or NIPT) ordered through her OB/Gyn after a discussion of all her prenatal screening options. She was referred to a genetic counselor to discuss her results in detail and options available
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During the Appointment Ann’s genetic counselor explained that her prenatal screening results indicated that her pregnancy had a higher chance of being affected with Down syndrome Ann discussed these results with her genetic counselor as well as possible next steps, which could include a diagnostic procedure (such as amniocentesis) for a prenatal diagnosis
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Moving Forward After meeting with her genetic counselor, Ann decided to have an amniocentesis, a diagnostic test, that indicated that her pregnancy does have trisomy 21 or Down syndrome. Ann can use the information from the amnio to determine the next best steps for her and her partner. This may include delivering at a high-risk hospital instead of her local hospital and preparing herself and her family for having a baby who will have special needs
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Cardiac Genetics
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Meet William A 50-year-old man comes to clinic after an echocardiogram revealed he had an enlarged aorta He had heard that some type of heart condition affected his relative, but he hadn’t realized he could be at risk since he felt healthy Now, he would like to learn more about his personal and family’s risks
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William’s Initial Family History
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During the Appointment We learned that his two deceased siblings had both passed away due to major medical problems with their aortas These events had been explained away due to pregnancy or drowning, so the emerging pattern was not immediately clear William was offered genetic testing for heritable thoracic aortic disease
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William’s Family History After Genetic Counseling
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Moving Forward William can work with his genetic counselor and family to determine whether he wants to pursue testing A positive test could allow his children to obtain testing themselves and obtain proper screening and medical care
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General Genetics
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Meet Gianna A 28-year-old woman, Gianna, comes to General Genetics clinic, with a history of chronic pain She had been to many other doctors’ appointments, and had been told that her symptoms were likely psychiatric Gianna also has a history of depression and anxiety Many “chronic pain” cases do not have a genetic explanation, however certain symptoms may suggest a genetic cause
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During the appointment... Genetic counselor asks for full, detailed history of pain, and Gianna explains she has severe stomach pain, and she often feels like hands and feet are burning or tingling The genetic counselor reviews medical records, and notices that in a routine urine test, Gianna was noted to have protein in her urine Gianna was adopted, and does not know any health information about her biological family
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Gianna’s Diagnosis Gianna is offered testing for Fabry disease, which confirms her diagnosis This condition has treatment, which helps Gianna’s symptoms improve Her diagnostic information can also be used for family planning, if Gianna is considering pregnancy
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Moving Forward Gianna’s genetic counselor gives her a flyer for a national Fabry support group, which she joins and meets other people with the same condition She is started on enzyme replacement therapy infusions every other week, which improves her symptoms Gianna is grateful that her genetic counselor took her concerns seriously, listened to her story and advocated for her
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Laboratory
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In a Genetic Testing Laboratory Phone call from a physician at a high-risk breast cancer clinic Patient is 52-year-old woman, who has never had cancer She had genetic testing 4 years ago at another doctor’s office, which revealed a variant of uncertain significance (VUS) in a gene called BRCA1
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In a Genetic Testing Laboratory Family history: Patient’s mother was diagnosed with breast cancer at 55, sister diagnosed with breast cancer at 45 Physician calls the lab to speak with a genetic counselor, and asks if additional genetic testing is necessary
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During the Phone Call Laboratory genetic counselor notes that a previously-reported variant of unknown significance (VUS) has now been reclassified as a “pathogenic variant” There are established medical guidelines to guide medical management, such as additional surveillance or surgery In addition, now specific testing may be offered to other, at-risk family members
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