Literature DB >> 30680851

Cases from the Undiagnosed Diseases Network: The continued value of counseling skills in a new genomic era.

Ellen F Macnamara1, Kelly Schoch2, Emily G Kelley3, Elizabeth Fieg4, Elly Brokamp5, Rebecca Signer6, Kimberly LeBlanc3, Allyn McConkie-Rosell2, Christina G S Palmer6,7,8.   

Abstract

The "diagnostic odyssey" is well known and described in genetic counseling literature. Studies addressing the psychological, emotional, and financial costs of not having a diagnosis have shown how it permeates the lives of patients and families. The Undiagnosed Diseases Network aims to end this odyssey by providing diagnoses to individuals with undiagnosed conditions through multidisciplinary evaluations, whole exome and genome sequencing, and basic science research. It also provides an opportunity to learn from patients and families and to better understand their journeys and the impact of receiving a diagnosis. Seven cases are presented that outline challenges that come from working with chronically undiagnosed and newly diagnosed patients in a time when sequencing for clinical diagnosis is rapidly increasing. They illuminate the emotional journey of patients and families searching for a diagnosis and the mental health problems, financial distress, and chaos that can accompany not having answers. They also illustrate the surprising reactions patients and families can have to receiving a diagnosis, including anger, grief, and disappointment. While the lessons learned from these families are not novel, new strategies are presented for handling these challenges in undiagnosed and ultra-rare populations, groups that will increase with the rise of clinical sequencing.
© 2019 National Society of Genetic Counselors.

Entities:  

Keywords:  WES/WGS; case vignettes; grief; psychosocial; rare disease

Mesh:

Year:  2019        PMID: 30680851      PMCID: PMC6456366          DOI: 10.1002/jgc4.1091

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.537


  29 in total

1.  Living without a diagnosis: the parental experience.

Authors:  Celine Lewis; Heather Skirton; Ray Jones
Journal:  Genet Test Mol Biomarkers       Date:  2010-10-12

2.  The NIH Undiagnosed Diseases Program: lessons learned.

Authors:  William A Gahl; Cynthia J Tifft
Journal:  JAMA       Date:  2011-05-11       Impact factor: 56.272

3.  Exploring the genetic counselor's role in facilitating meaning-making: rare disease diagnoses.

Authors:  Benjamin M Helm
Journal:  J Genet Couns       Date:  2015-01-08       Impact factor: 2.537

4.  Long-term psychological consequences of pregnancy termination for fetal abnormality: a cross-sectional study.

Authors:  M J Korenromp; G C M L Christiaens; J van den Bout; E J H Mulder; J A M Hunfeld; C M Bilardo; J P M Offermans; G H A Visser
Journal:  Prenat Diagn       Date:  2005-03       Impact factor: 3.050

5.  "Is it going to hurt?": the impact of the diagnostic odyssey on children and their families.

Authors:  Nikkola Carmichael; Judith Tsipis; Gail Windmueller; Leslie Mandel; Elicia Estrella
Journal:  J Genet Couns       Date:  2014-10-04       Impact factor: 2.537

6.  Whole Exome Sequencing in Pediatric Neurology Patients: Clinical Implications and Estimated Cost Analysis.

Authors:  Danielle Nolan; Martha Carlson
Journal:  J Child Neurol       Date:  2016-02-10       Impact factor: 1.987

7.  Obtaining a genetic diagnosis in a child with disability: impact on parental quality of life.

Authors:  M Lingen; L Albers; M Borchers; S Haass; J Gärtner; S Schröder; L Goldbeck; R von Kries; K Brockmann; B Zirn
Journal:  Clin Genet       Date:  2015-07-14       Impact factor: 4.438

8.  Clinical exome sequencing for genetic identification of rare Mendelian disorders.

Authors:  Hane Lee; Joshua L Deignan; Naghmeh Dorrani; Samuel P Strom; Sibel Kantarci; Fabiola Quintero-Rivera; Kingshuk Das; Traci Toy; Bret Harry; Michael Yourshaw; Michelle Fox; Brent L Fogel; Julian A Martinez-Agosto; Derek A Wong; Vivian Y Chang; Perry B Shieh; Christina G S Palmer; Katrina M Dipple; Wayne W Grody; Eric Vilain; Stanley F Nelson
Journal:  JAMA       Date:  2014-11-12       Impact factor: 56.272

9.  A prospective study on parental coping 4 months after termination of pregnancy for fetal anomalies.

Authors:  M J Korenromp; G C M L Page-Christiaens; J van den Bout; E J H Mulder; J A M Hunfeld; C M A A Potters; J J H M Erwich; C J M van Binsbergen; J T J Brons; J R Beekhuis; A W J Omtzigt; G H A Visser
Journal:  Prenat Diagn       Date:  2007-08       Impact factor: 3.050

10.  Prospective comparison of the cost-effectiveness of clinical whole-exome sequencing with that of usual care overwhelmingly supports early use and reimbursement.

Authors:  Zornitza Stark; Deborah Schofield; Khurshid Alam; William Wilson; Nessie Mupfeki; Ivan Macciocca; Rupendra Shrestha; Susan M White; Clara Gaff
Journal:  Genet Med       Date:  2017-01-26       Impact factor: 8.822

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  6 in total

1.  Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG).

Authors:  Kandamurugu Manickam; Monica R McClain; Laurie A Demmer; Sawona Biswas; Hutton M Kearney; Jennifer Malinowski; Lauren J Massingham; Danny Miller; Timothy W Yu; Fuki M Hisama
Journal:  Genet Med       Date:  2021-07-01       Impact factor: 8.822

2.  Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases.

Authors:  Shilpa Nadimpalli Kobren; Dustin Baldridge; Matt Velinder; Joel B Krier; Kimberly LeBlanc; Cecilia Esteves; Barbara N Pusey; Stephan Züchner; Elizabeth Blue; Hane Lee; Alden Huang; Lisa Bastarache; Anna Bican; Joy Cogan; Shruti Marwaha; Anna Alkelai; David R Murdock; Pengfei Liu; Daniel J Wegner; Alexander J Paul; Shamil R Sunyaev; Isaac S Kohane
Journal:  Genet Med       Date:  2021-02-12       Impact factor: 8.822

3.  Receiving Genomic Sequencing Results through the Victorian Undiagnosed Disease Program: Exploring Parental Experiences.

Authors:  Jo Martinussen; Michal Chalk; Justine Elliott; Lyndon Gallacher
Journal:  J Pers Med       Date:  2022-07-29

4.  Clinical application of a scale to assess genomic healthcare empowerment (GEmS): Process and illustrative case examples.

Authors:  Allyn McConkie-Rosell; Kelly Schoch; Jennifer Sullivan; Rebecca C Spillmann; Heidi Cope; Queenie K-G Tan; Christina G S Palmer; Stephen R Hooper; Vandana Shashi
Journal:  J Genet Couns       Date:  2021-06-11       Impact factor: 2.537

5.  Abnormal expression of GABAA receptor subunits and hypomotility upon loss of gabra1 in zebrafish.

Authors:  Nayeli G Reyes-Nava; Hung-Chun Yu; Curtis R Coughlin; Tamim H Shaikh; Anita M Quintana
Journal:  Biol Open       Date:  2020-04-13       Impact factor: 2.422

Review 6.  Current Status of Genetic Counselling for Rare Diseases in Spain.

Authors:  Sara Álvaro-Sánchez; Irene Abreu-Rodríguez; Anna Abulí; Clara Serra-Juhe; Maria Del Carmen Garrido-Navas
Journal:  Diagnostics (Basel)       Date:  2021-12-09
  6 in total

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