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

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.

[1]  T. Shaikh,et al.  Abnormal expression of GABAA receptor subunits and hypomotility upon loss of gabra1 in zebrafish , 2020, Biology Open.

[2]  M. Crimi,et al.  Experiences of patients with Poland syndrome of diagnosis and care in Italy: a pilot survey , 2019, Orphanet Journal of Rare Diseases.

[3]  Rebecca C. Spillmann,et al.  Psychosocial Profiles of Parents of Children with Undiagnosed Diseases: Managing Well or Just Managing? , 2018, Journal of Genetic Counseling.

[4]  Sharyn A. Lincoln,et al.  Understanding Adult Participant and Parent Empowerment Prior to Evaluation in the Undiagnosed Diseases Network , 2018, Journal of Genetic Counseling.

[5]  B. Biesecker,et al.  Factors Associated with Parental Adaptation to Children with an Undiagnosed Medical Condition , 2017, Journal of Genetic Counseling.

[6]  Matthew H. Brush,et al.  A window into living with an undiagnosed disease: illness narratives from the Undiagnosed Diseases Network , 2017, Orphanet Journal of Rare Diseases.

[7]  J. Christodoulou,et al.  Australian children living with rare diseases: experiences of diagnosis and perceived consequences of diagnostic delays , 2017, Orphanet Journal of Rare Diseases.

[8]  Clara Gaff,et al.  Prospective comparison of the cost-effectiveness of clinical whole-exome sequencing with that of usual care overwhelmingly supports early use and reimbursement , 2017, Genetics in Medicine.

[9]  D. L. Doyle,et al.  2013 Review and Update of the Genetic Counseling Practice Based Competencies by a Task Force of the Accreditation Council for Genetic Counseling , 2016, Journal of Genetic Counseling.

[10]  William A Gahl,et al.  The NIH Undiagnosed Diseases Program and Network: Applications to modern medicine. , 2016, Molecular genetics and metabolism.

[11]  Martha Carlson,et al.  Whole Exome Sequencing in Pediatric Neurology Patients , 2016, Journal of Child Neurology.

[12]  M. Lingen,et al.  Obtaining a genetic diagnosis in a child with disability: impact on parental quality of life , 2016, Clinical genetics.

[13]  B. Fernandez,et al.  Utility of whole‐exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care , 2015, Clinical genetics.

[14]  B. Meiser,et al.  Mothers’ psychological adaptation to Duchenne/Becker muscular dystrophy , 2015, European Journal of Human Genetics.

[15]  K. Harmon,et al.  Stages of psychological impact after diagnosis with serious or potentially lethal cardiac disease in young competitive athletes: a new model. , 2015, Journal of electrocardiology.

[16]  E. Estrella,et al.  “Is it Going to Hurt?”: The Impact of the Diagnostic Odyssey on Children and Their Families , 2015, Journal of Genetic Counseling.

[17]  B. Helm Exploring the Genetic Counselor’s Role in Facilitating Meaning-Making: Rare Disease Diagnoses , 2015, Journal of Genetic Counseling.

[18]  Eric Vilain,et al.  Clinical exome sequencing for genetic identification of rare Mendelian disorders. , 2014, JAMA.

[19]  Magalie S Leduc,et al.  Clinical whole-exome sequencing for the diagnosis of mendelian disorders. , 2013, The New England journal of medicine.

[20]  Allyn McConkie-Rosell,et al.  The utility of the traditional medical genetics diagnostic evaluation in the context of next-generation sequencing for undiagnosed genetic disorders , 2013, Genetics in Medicine.

[21]  B. V. van Bon,et al.  Diagnostic exome sequencing in persons with severe intellectual disability. , 2012, The New England journal of medicine.

[22]  B. Bernhardt,et al.  Factors associated with perceived uncertainty among parents of children with undiagnosed medical conditions , 2012, American journal of medical genetics. Part A.

[23]  Kelly Schoch,et al.  Clinical application of exome sequencing in undiagnosed genetic conditions , 2012, Journal of Medical Genetics.

[24]  C. Tifft,et al.  The NIH Undiagnosed Diseases Program: lessons learned. , 2011, JAMA.

[25]  Ray B. Jones,et al.  Living without a diagnosis: the parental experience. , 2010, Genetic testing and molecular biomarkers.

[26]  J. R. Beekhuis,et al.  A prospective study on parental coping 4 months after termination of pregnancy for fetal anomalies , 2007, Prenatal diagnosis.

[27]  R. Bennett,et al.  A New Definition of Genetic Counseling: National Society of Genetic Counselors’ Task Force Report , 2006, Journal of Genetic Counseling.

[28]  J. van den Bout,et al.  Long‐term psychological consequences of pregnancy termination for fetal abnormality: a cross‐sectional study , 2005, Prenatal diagnosis.

[29]  L. Biesecker,et al.  Parental attitudes toward a diagnosis in children with unidentified multiple congenital anomaly syndromes. , 2001, American journal of medical genetics.

[30]  G. Lortie,et al.  Parental reaction and adaptability to the prenatal diagnosis of fetal defect or genetic disease leading to pregnancy interruption , 1995, Prenatal diagnosis.

[31]  A. Vanputte Perinatal bereavement crisis: coping with negative outcomes from prenatal diagnosis. , 1988, The Journal of perinatal & neonatal nursing.