Gotowe bibliografie tematyczne / Genetic counseling – Psychological aspects

Gotowa bibliografia na temat „Genetic counseling – Psychological aspects”

Autor: Grafiati

Data publikacji: 4 czerwca 2021

Data aktualizacji: 1 lutego 2022

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Artykuły w czasopismach na temat "Genetic counseling – Psychological aspects"

Kessler, Seymour. "Psychological Aspects of Genetic Counseling. X. Advanced Counseling Techniques". Journal of Genetic Counseling 6, nr 4 (grudzień 1997): 379–92. http://dx.doi.org/10.1023/a:1025644825912.

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Kessler, Seymour. "Psychological Aspects of Genetic Counseling. IX. Teaching and Counseling". Journal of Genetic Counseling 6, nr 3 (wrzesień 1997): 287–95. http://dx.doi.org/10.1023/a:1025676205440.

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Kessler, Seymour. "Psychological Aspects of Genetic Counseling: XII. More on Counseling Skills". Journal of Genetic Counseling 7, nr 3 (czerwiec 1998): 263–78. http://dx.doi.org/10.1023/a:1022895207096.

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Kessler, Seymour. "Psychological Aspects of Genetic Counseling. XIV. Nondirectiveness and Counseling Skills". Genetic Testing 5, nr 3 (wrzesień 2001): 187–91. http://dx.doi.org/10.1089/10906570152742227.

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Sharpe, Neil F. "Psychological aspects of genetic counseling: A legal perspective". American Journal of Medical Genetics 50, nr 3 (15.04.1994): 234–38. http://dx.doi.org/10.1002/ajmg.1320500305.

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Kessler, Seymour. "Psychological aspects of genetic counseling. XI. Nondirectiveness revisited". American Journal of Medical Genetics 72, nr 2 (17.10.1997): 164–71. http://dx.doi.org/10.1002/(sici)1096-8628(19971017)72:2<164::aid-ajmg8>3.0.co;2-v.

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Kessler, Seymour. "Psychological Aspects of Genetic Counseling: XIII. Empathy and Decency". Journal of Genetic Counseling 8, nr 6 (grudzień 1999): 333–43. http://dx.doi.org/10.1023/a:1022967208933.

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Kessler, Seymour. "Psychological aspects of genetic counseling. VII. Thoughts on directiveness". Journal of Genetic Counseling 1, nr 1 (marzec 1992): 9–17. http://dx.doi.org/10.1007/bf00960080.

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Kessler, Seymour. "Psychological aspects of genetic counseling. VIII. Suffering and countertransference". Journal of Genetic Counseling 1, nr 4 (grudzień 1992): 303–8. http://dx.doi.org/10.1007/bf00962826.

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Kessler, Seymour, Eleanor K. Levine, John M. Opitz i James F. Reynolds. "Psychological aspects of genetic counseling: IV. The subjective assessment of probability". American Journal of Medical Genetics 28, nr 2 (październik 1987): 361–70. http://dx.doi.org/10.1002/ajmg.1320280214.

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Rozprawy doktorskie na temat "Genetic counseling – Psychological aspects"

Hayat, Roshanai Afsaneh. "Psychological and Behavioral Aspects of Receiving Genetic Counseling for Hereditary Cancer". Doctoral thesis, Uppsala universitet, Vårdvetenskap, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-128870.

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The overall aims of this thesis were to investigate psychological and behavioral effects of receiving cancer genetic counseling for breast, ovarian and colorectal cancer and/or with a family history of these cancer types and to determine whether counselees’ informational needs were met. Study I was performed 3-7 years post-counseling. Participants (n=214) reported a relatively high level of anxiety but a low level of depression compared to cancer patients in general. However, there was no indication that the distress experienced was due to the counseling. Moderate changes in life and family relations, high level of adherence to recommended controls and satisfaction was reported. Study II was a randomized control trial (RCT) intervention study which involved 147 counselees. An increase in the level of knowledge and correct estimation of personal risk was reported in both the intervention and control groups, although this increase declined at later follow-up. Enhanced information led to significantly greater satisfaction with the given information, and the way of informing relatives. Most counselees had shared information with their at-risk relatives. Study III focused on sharing information with at-risk relatives among participants in study II and their relatives (n=81). Counselees were interviewed and answered a questionnaire, whilst their relatives only answered the questionnaire. Counselees reported positive/neutral feelings about communicating genetic information and mostly interpreted their relatives’ reactions as positive/ neutral. Also, approximately 50% of relatives reported positive/neutral reactions and were generally satisfied with the received information. Study IV was conducted in Sweden and Norway based on 235 counselees. Counselees expected counselors to be skillful and thoughtful, take them seriously and provide risk estimations and medical information. Most important issues to counselees were satisfactorily addressed by the counselors. Analyzing importance rankings resulted in five categories of needs: a need for facts, caring communication and medical information, need for understanding and support in sharing genetic information, practical care and medical/practical information. In conclusion, no adverse psychological or behavioral effect on counselees was observed. Apparently, genetic counseling is managed properly and counselors successfully address counselees’ needs. Providing extended information does not seem necessary, however, tailoring information to individual counselees needs may create a more effective counseling.

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Tedgård, Ulf. "Prenatal diagnosis of haemophilia psychological, social and ethical aspects /". Malmö : Dept. of Pediatrics, University Hospital of Malmö, University of Lund, 1999. http://catalog.hathitrust.org/api/volumes/oclc/57455671.html.

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Wade, Walsh Margo. "Women Receiving Genetic Counseling for Breast Cancer Risk: Cancer Worry, Psychological Distress, and Risk Recall Accuracy". Thesis, University of North Texas, 1999. https://digital.library.unt.edu/ark:/67531/metadc2185/.

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This follows an earlier study of the same data set, which, through its findings, presented new questions that are investigated in this study. Both studies used a prospective controlled design, wherein women receiving genetic counseling for breast cancer risk were randomized into two groups. Subjects receiving an audiotaped recording of their genetic consultation (tape group) were compared to subjects who also had a genetic consultation but did not receive an audiotaped recording of it (no-tape group). Participants were drawn from attendees at the genetic clinics of two London hospitals and included 115 women with a family history of breast cancer. Cancer worry and psychological distress were assessed before genetic consultation (baseline), and at one- and six-month follow-ups by post. Objective risk was estimated by the geneticist during the consultation, and subjective risk was assessed at one month follow-up. The goals of the current study were to investigate relationships between cancer worry, psychological distress, and recall of genetic risk for breast cancer in a sample of women receiving genetic counseling for breast cancer risk, and to investigate the role sociodemographic variables on cancer worry, psychological distress, or risk recall for these women. Results for this sample of women with a family history of breast cancer found that there were consistent relationships between cancer worry, psychological distress, objective risk, and subjective risk before and after genetic consultation. This suggests that women=s psychological responses are appropriate to their level of cancer risk. There were no differences found between the tape and no-tape groups for objective or subjective risk, or for nearness of recall accuracy or degree of under-/over-estimation. Provision of an audiotaped recording of the genetic consultation did not appear to enhance recall of risk information. The role of sociodemographic variables on the psychological and risk variables assessed in this study was very minor. Age was mildly correlated with cancer worry, and employment was predictive of cancer worry only at baseline.

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Williamson, Nancy D. "Psychological Responses of Fathers and Mothers to Amniocentesis". Master's thesis, University of Central Florida, 1985. http://digital.library.ucf.edu/cdm/ref/collection/RTD/id/15675.

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University of Central Florida College of Arts and Sciences Thesis
Amniocentesis is one of the most widely used prenatal diagnostic techniques for congenital disorders. It was hypothesized that the spychological responses of mothers and fathers to amniocenthesis during high-rish pregnancies would be positively correlated on scales of Symptomatology (Anxiety, Depression, Anger, and Somatic Complaints) and Well-Being (Relaxed, Contented, Friendliness, and Somatic Well-Being). It was also hypothesized that Symptomatology would be negatively correlated with Well-Being. Nineteen couples, who were referred by their physicians, voluntarily participated in the study. Each partner completed the Symptom Questionnaire (Kellner, 1983), a self-rating scale of Symptomatology and Well-Being, in addition to the Pre-Amniocentesis and Post-Amniocentesis Questionnaires (original questionnaires developed for this study) at intervals prior to and following the procedure, while awaiting results. A Pearson product-moment correlation of the total scores revealed a positive correlation (p < 0.5) between the scores of fathers and mothers on the Symptomatology Scale, both pre- and post-amniocentesis (r = .47 and .47). In addition, there was a significant negative correlation (p < .05) between Symptomatolgy and Well-Being scores for both mothers (r = -.55 and -.60) and fathers (r = -.48 and -.74) at the pre- and post-amniocentesis periods, respectively. The hypothesis cannot be completely accepted because the positive correlation does not exist at the post-amniocentesis level. Mothers appear to experience more Symptomatology and less Well-Being than fathers at the post-amniocentesis level. The results are interpreted to suggest that fathers and mothers may both benefit from pre- and post-amniocentesis supportive intervention.
M.S.;
Masters
Arts and Sciences;
Clinical Psychology;
42 p.
vii, 42 leaves, bound : ill. ; 28 cm.

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Elliott, Diana. "The impact of genetic counselling for familial breast cancer on women's psychological distress, risk perception and understanding of BRCA testing". University of Western Australia. School of Population Health, 2008. http://theses.library.uwa.edu.au/adt-WU2008.0190.

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[Truncated abstract] Background: A review of the literature indicated there was a need for more long-term randomised controlled studies on the effects of BRCA counselling/testing on high risk women, including improved strategies for risk communication. Reviews have also shown women are confused about the significance of inconclusive or non informative results with a need for more research in this area. Aims: The general aim of this study was to evaluate the impact of breast cancer genetic counselling on psychological distress levels, perception of risk, genetic knowledge and understanding of BRCA testing/test results in a cohort of 207 women from high risk breast cancer families who were referred for genetic counselling in Perth during the period 1997 to 2001. Short- and long-term impact of BRCA genetic counselling/testing was determined in women with and without cancer in a randomised controlled trial as part of which women were randomised to either receive immediate versus delayed genetic counselling. This included family communication patterns before BRCA testing, anticipated outcomes of testing on oneself and family including intentions for result disclosure. Comprehension of index and predictive BRCA testing with possible results was assessed both in the short- and the long-term and understanding of individual or family BRCA test results was evaluated at long-term. The effect of genetic counselling on breast cancer risk perception in unaffected women was evaluated. This study considered a theoretical framework of educational learning theories to provide a basis for risk communication with possible relevance for future research. ... Only 25% of the original study population (52/207) reported BRCA results and women's understanding of results is concerning. Key findings were: 1. The majority of affected women received an inconclusive result. 2. Out of twelve unaffected women who reported results, seven were inconclusive which are not congruent with predictive testing. This implies that these women did not understand their test result. 3. A minority of untested relatives did not know whether a family mutation had or had not been found in their tested family member or what their actual test result was. This implies either a lack of disclosure or that woman did not understand the rationale for and significance of testing for a family mutation. 4. Three relatives did not understand a positive result was a mutation. Conclusion: The implication of this research for breast cancer counselling and testing services is that women who wait for counselling are no worse off in terms of short- or long-term general psychological distress than women who receive the intervention early. There is a suggestion that unaffected women without the disease found counselling more advantageous than affected women. The meaning of BRCA results as reported by women is concerning particularly women's understanding of negative and inconclusive results and further research is needed in this area. Too much information presented at counselling may affect women's comprehension of risk, BRCA testing and future test results and further research is required to evaluate the effects of information overload.

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Steggles, Naomi. "Psychological aspects of genetic testing for cancer". Thesis, University College London (University of London), 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.271020.

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Lesniak, Karen. "Psychological and Sociodemographic Predictors of Psychological Distress in BRCA1 and BRCA2 Genetic Testing Participants within a Community Based Genetic Screening Program". Thesis, University of North Texas, 2000. https://digital.library.unt.edu/ark:/67531/metadc2565/.

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Mutations in BRCA1 and BRCA2, the first two breast cancer susceptibility genes identified, carry as much as an 85% lifetime risk of developing breast, ovarian or other cancers. Genetic testing for mutations in these two genes has recently become commercially available. There have been varying amounts of psychological distress noted among women with a family history of breast cancer. Distress has been observed to impact psychological functioning, activities of daily living, and the practice of breast cancer surveillance behaviors. Within the genetic screening process, psychological distress has been shown to impact the decision to undergo genetic screening, the comprehension and retention of risk assessment information, as well as affecting the subject following the receipt of the genetic test results. Little work has been done to examine predictors of distress within at risk subjects. This study examines psychological distress among 52 community women presenting for BRCA1 and BRCA2 genetic mutation testing. Predictors of distress included family cancer history, education, age, Ashkenazi ethnicity, and Internality and Powerful Others Health Locus of Control. Vulnerable sub-groups of patients include younger women, women with higher levels of education and women of Ashkenazi ethnicity.

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Liu, Pak-yin Anthony, i 廖柏賢. "Genetic counseling in sudden arrhythmia death syndrome : the science and the art". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2013. http://hdl.handle.net/10722/196059.

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Background: Sudden arrhythmia death syndrome (SADS) is a genotypically and phenotypically heterogeneous condition that might produce fatal ventricular arrhythmia in otherwise healthy individuals. Congenital long QT syndrome (LQTS) is the most common type of SADS with a frequency of 1 in 2500 individuals. Up to 13 genes have been shown to be associated with LQTS and genetic testing has a role in disease diagnosis, prognostication, treatment guidance, cascade testing, and reproductive counseling. Interdisciplinary care is the standard but such service is unavailable in Hong Kong. Objectives: In this study, we aim to evaluate the clinical characteristics of a local cohort of pediatric patients with LQTS, establish the practicability of a model on interdisciplinary delivery of care for SADS, and explore the process of genetic counseling in Chinese families with LQTS from the perspective of discourse analysis. Method: Pediatric patients with LQTS and their families were recruited from the Department of Paediatric Cardiology, Queen Mary Hospital between 1 January 2011 and 31 December 2012. With informed consent, patients underwent genetic testing for 6 LQTS genes (KCNQ1, KCNH2, SCN5A, KCNE1, KCNE2, KCNJ2). Clinical characteristics were documented and the process of pre-test and post-test counseling was videotaped and transcribed. Data was mapped and analyzed for discourse strategies in the focal themes of uncertainty management in risk communication. Results: 19 patients were identified, 9 were male, with the corrected QT interval (QTc) ranging from 460-619ms. Mode of presentation included syncope (n=9), ventricular tachycardia (n=2), convulsion (n=1) and as incidental finding (n=7). Pathogenic mutations were identified in 9 patients (LQT1=3, LQT2=4, LQT3=1, LQT5=1), likely pathogenic mutations in 2 (LQT2), unclassified variants in 2, and no mutation in 6. Patients with pathogenic and likely pathogenic mutations had significantly longer mean QTc than those without such mutations (p=0.046). Three mutations, all in the LQT2 genes, represented novel mutations. All 3 patients with mutations in the pore-looping forming domains of the KCNH2 (LQT2) channel had personal or family histories of malignant arrhythmia or sudden cardiac death compatible with previously reported genotype-phenotype correlation. Eight families involving 18 family members underwent cascade testing, and family mutations were identified in 10 individuals from 6 families. Autosomal dominant transmission was the likely mode of inheritance in these 6 families. Counseling sessions involved the joint input from clinical geneticist, genetic counsellor and pediatric cardiologist. Discourse analysis on 2 counseling sessions of a selected family with unclassified variants revealed increased uncertainty after genetic testing in the index patient and family members. Strategies used to mitigate uncertainty included abstraction, generalization and categorization. Conclusion: Genetic testing was crucial in the comprehensive assessment of patients with congenital LQTS, and we demonstrated a feasible model to delivery interdisciplinary care for patients with SADS in Hong Kong. The process of genetic counseling is highly complex and deserves further examination.
published_or_final_version
Paediatrics and Adolescent Medicine
Master
Master of Medical Sciences

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Pisano, Bonnie S. "Late luteal phase dysphoric disorder symptoms (PMS) among women presenting for counseling services". Virtual Press, 1990. http://liblink.bsu.edu/uhtbin/catkey/720149.

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Changes in mood, behavior, and physiology, beginning in the post-ovulatory phase of the menstrual cycle and ending with the onset of menstruation, have been called premenstrual syndrome, or PMS, and have been the focus of much investigation. Research to date has demonstrated greater emotional arousal and distress experienced by women during the luteal phase of the cycle as opposed to the follicular phase. This study collected descriptive profiles of current mood states, physiological symptoms, and menstrual cycle information from 62 women on the day on which they presented to a university counseling center for psychological services. It was hypothesized that a larger proportion of individuals would present on a walk-in basis for intake during the luteal phase of the cycle as opposed to the follicular phase. This hypothesis was tested with Chi-Square analysis of differences in frequency of subjects in each of the two phase groups. The second hypothesis was that individuals in the luteal phase would display higher levels of mood disturbance (as measured by the Profile of Mood States and the Beck Depression Inventory) and somatic symptomatology (as measured by the Menstrual Cycle Symptom Scale),than individuals in the follicular phase. This hypothesis was tested using multiple regression analysis, using affective and somatic variables as predictors of cycle day. Post hoc analyses for differences between menstrual phase groups on the affective variables were performed using multivariate analysis of variance (MANOVA).The results of this study indicated no relationship between menstrual cycle phase and self-presentation for counseling services. They also indicated no relationship between menstrual cycle day and either subjective distress or somatic symptomatology. Finally, with minor exceptions, no differences were found between menstrual cycle phase groups in their self-perceived distress or emotional states.Discrepancies between the results of this study and previous research were discussed. In particular, methodological differences (e.g., use of state vs trait measures of mood variables) highlight the poor design and generalizability of previous research. Suggestions for future studies were presented as well as limiting factors in this study. These include the need for a larger number of participants and the use of hematologic cross-checks to more precisely determine cycle phase. Investigations into the way in which menstrual cycle affects mood are warranted.
Department of Counseling Psychology and Guidance Services

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Schmidt, Mellis I. (Mellis Irene). "Forgiveness as the Focus Theme in Group Counseling". Thesis, North Texas State University, 1986. https://digital.library.unt.edu/ark:/67531/metadc330735/.

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This study reviewed the literature regarding forgiveness and developed a structured group counseling format with the theme of forgiveness. The purpose of the study was to determine the effect of forgiveness as used in group counseling upon depression, generalized anxiety, dogmatism, relationships, guilt, and forgiveness in the participants. Thirty subjects were selected to participate in one of three groups: an experimental group, a comparison treatment group, and a control group. The experimental group and the comparison treatment group participated in two-hour group sessions, once a week for ten weeks. The experimental group was didactic and experiential with the focus on forgiveness, whereas the comparison treatment group was problem solving using Redecision Therapy. All groups participated in pre and post test sessions. The seven hypotheses in this study were tested with a multivariate analysis of covariance as well as univariate analysis of covariance for each hypothesis. Significance in differences between means was tested at the .05 level of significance.

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Książki na temat "Genetic counseling – Psychological aspects"

G, Resta Robert, red. Psyche and helix: Psychological aspects of genetic counseling : essays. New York: Wiley-Liss, 2000.

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Counseling about cancer: Strategies for genetic counseling. Wyd. 2. New York: Wiley-Liss, 2002.

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Schneider, Katherine A. Counseling about cancer: Strategies for genetic counselors. Wyd. 2. New York: Wiley-Liss, 2002.

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Schneider, Katherine A. Counseling about cancer: Strategies for genetic counselors. Dennisport, Mass: Graphic Illusions, 1994.

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1947-, Burke B. Meredith, red. Prenatal testing: A sociological perspective. Westport, Conn: Bergin & Garvey, 1994.

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Barbara, Biesecker, red. Genetic counselling: A psychological conversation. Cambridge, UK: Cambridge University Press, 2006.

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G, Marchese Sandra, red. Genetic counseling for clinicians. Chicago: Year Book Medical Publishers, 1986.

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Counseling about cancer: Strategies for genetic counseling. Wyd. 3. Hoboken, N.J: Wiley-Blackwell, 2012.

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Sommer, Annemarie. Birth defects and genetic screening and counseling. Washington, D.C: Veterans Administration Central Office, Dept. of Medicine and Surgery, Agent Orange Projects Office, 1985.

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Sommer, Annemarie. Birth defects and genetic screening and counseling. Washington, D.C: Veterans Administration Central Office, Dept. of Medicine and Surgery, Agent Orange Projects Office, 1985.

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Części książek na temat "Genetic counseling – Psychological aspects"

Aspinwall, Lisa G., Jennifer M. Taber, Wendy Kohlmann i Sancy A. Leachman. "Psychological Aspects of Hereditary Cancer Risk Counseling and Genetic Testing". W Psychological Aspects of Cancer, 31–64. Boston, MA: Springer US, 2012. http://dx.doi.org/10.1007/978-1-4614-4866-2_3.

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Di Mattei, Valentina, Martina Bernardi i Letizia Carnelli. "Psychological distress and other aspects regarding cancer genetic testing". W Counseling and Coaching in Times of Crisis and Transition, 206–17. Abingdon, Oxon ; New York, NY : Routledge, 2018.: Routledge, 2017. http://dx.doi.org/10.4324/9781315266596-18.

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Foretová, Lenka, i Tomá š. Skřička. "Psychological and Medico-Legal Aspect of Genetic Counseling in Familial Adenomatous Polyposis". W Intestinal Polyps and Polyposis, 217–24. Milano: Springer Milan, 2009. http://dx.doi.org/10.1007/978-88-470-1124-3_21.

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Esplen, M. J. "Psychological Aspects". W Genetic Testing, 53–78. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2006. http://dx.doi.org/10.1002/0471748897.ch3.

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Garicochea, Bernardo, i Rodrigo Santa Cruz Guindalini. "Practical Aspects of Genetic Counseling: Genetic Tests to Identify Risks". W Breast Diseases, 191–97. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-13636-9_21.

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Yaghmaie, Marjan, Mohammad Ahmadvand, Ali-akbar Nejati Safa i Hossein Pashaiefar. "Genetic, Hematologic and Psychological Aspects of Leukemia". W Cancer Genetics and Psychotherapy, 667–755. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-64550-6_14.

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De Geus, Eco J. C., i Marleen H. M. De Moor. "Genes, Exercise, and Psychological Factors". W Genetic and Molecular Aspects of Sport Performance, 294–305. Oxford, UK: Wiley-Blackwell, 2010. http://dx.doi.org/10.1002/9781444327335.ch25.

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Peterson, Susan K. "Psychological Impact of Genetic Counseling and Testing for Hereditary Colorectal Cancers". W Hereditary Colorectal Cancer, 559–73. Boston, MA: Springer US, 2010. http://dx.doi.org/10.1007/978-1-4419-6603-2_33.

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Sarkar, Rashmi, i Shilpa Garg. "Quality-of-Life Measures and Psychological Aspects in Vitiligo (Counseling and Support Groups)". W Comprehensive Textbook on Vitiligo, 99–104. First edition. | Boca Raton, FL : CRC Press, 2020.: CRC Press, 2020. http://dx.doi.org/10.1201/9781315112183-20.

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Makhnoon, Sukh, i Susan K. Peterson. "Psychosocial Issues in Genetic Testing for Hereditary Colorectal Cancer". W Psycho-Oncology, redaktor Paul B. Jacobsen, 102–9. Oxford University Press, 2021. http://dx.doi.org/10.1093/med/9780190097653.003.0015.

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Psychosocial factors influence colorectal cancer (CRC) genetic testing decisions and risk management strategies. Psychosocial research on hereditary CRC has focused on understanding individuals’ motivations and decisions regarding genetic testing, the psychological impact of genetic risk notification, the effects on family and interpersonal relationships, and factors influencing the uptake of risk reduction options (e.g., screening, risk-reducing surgery, or chemoprevention). Overall, the literature on psychosocial aspects of hereditary CRC suggest that despite initial fears, negative psychological impacts of genetic testing are often absent or modest, and adverse impacts, if observed, are short-lived. Due to the shared familial nature of genetic information, patients utilizing CRC genetic testing also experience novel psychosocial challenges in terms of family communication and childbearing. Positive psychosocial benefits such as relief from uncertainty and satisfaction of curiosity have been less frequently examined. Psychosocial outcomes vary across types of genetic testing, test results, gene penetrance and associated cancer risks, and various clinical and personal factors. For example, the psychosocial outcomes in response to an uncertain test result from a moderate-penetrance CRC-related gene may be different from a negative test result in a high-penetrance gene. This suggests that generalizing psychosocial outcomes from the various areas of scholarship may be unwise. Psychosocial aspects of genetic testing deserve attention by researchers and clinicians to design and deliver tailored genetic and psychological counseling support services geared to the ongoing needs of patients and their relatives who face genetic risk for colorectal cancer.

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Streszczenia konferencji na temat "Genetic counseling – Psychological aspects"

Carolina, Calaras. "Psycho-pedagogical counseling of the family as a factor in streamlining intergenerational communication and relationships". W Condiții pedagogice de optimizare a învățării în post criză pandemică prin prisma dezvoltării gândirii științifice. "Ion Creanga" State Pedagogical University, 2021. http://dx.doi.org/10.46728/c.18-06-2021.p226-230.

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The article contains a theoretical study with practical implications, which shows the specifics and content of family psycho-pedagogical counseling, approached as a factor in streamlining intergenerational communication and relationships. The characteristics of psycho-pedagogical counseling, its dimensions (psychological and pedagogical) and basic aspects, which require the attention of the specialist in the family counseling process in order to harmonize communication and family relationships, were listed and explained in an original way.

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