Literature DB >> 27894449

Ending a Diagnostic Odyssey: Family Education, Counseling, and Response to Eventual Diagnosis.

Donald Basel1, Julie McCarrier2.   

Abstract

Genomic sequencing is the diagnostic test of choice for families with undiagnosed or rare diseases seeking an explanation for their child's complex medical concerns. The desire to find answers can easily bias interpretation of sequencing results, and thus the counseling process is designed to facilitate informed decision making and set realistic expectations for possible outcomes. The patient case examples serve to highlight the various challenges and complexities encountered with the clinical application of genomic sequencing and to reflect some of the data that has been accrued during the past 5 years of clinical experience. Copyright Â
© 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Categorical model for WES results disclosure; Diagnostic odyssey; Genetic counseling; Patient experiences-Case series; Variant calling; Whole exome sequencing

Mesh:

Year:  2017        PMID: 27894449     DOI: 10.1016/j.pcl.2016.08.017

Source DB:  PubMed          Journal:  Pediatr Clin North Am        ISSN: 0031-3955            Impact factor:   3.278


  10 in total

1.  The diagnostic odyssey: insights from parents of children living with an undiagnosed condition.

Authors:  Alicia Bauskis; Cecily Strange; Caron Molster; Colleen Fisher
Journal:  Orphanet J Rare Dis       Date:  2022-06-18       Impact factor: 4.303

2.  A systematic literature review of disclosure practices and reported outcomes for medically actionable genomic secondary findings.

Authors:  Julie C Sapp; Flavia M Facio; Diane Cooper; Katie L Lewis; Emily Modlin; Philip van der Wees; Leslie G Biesecker
Journal:  Genet Med       Date:  2021-08-26       Impact factor: 8.864

3.  Hope versus reality: Parent expectations of genomic testing.

Authors:  Katherine E Donohue; Siobhan M Dolan; Dana Watnick; Katie M Gallagher; Jacqueline A Odgis; Sabrina A Suckiel; Nehama Teitelman; Bruce D Gelb; Eimear E Kenny; Melissa P Wasserstein; Carol R Horowitz; Laurie J Bauman
Journal:  Patient Educ Couns       Date:  2021-01-29

Review 4.  The Korean undiagnosed diseases program: lessons from a one-year pilot project.

Authors:  Soo Yeon Kim; Byung Chan Lim; Jin Sook Lee; Woo Joong Kim; Hyuna Kim; Jung Min Ko; Ki Joong Kim; Sun Ah Choi; Hunmin Kim; Hee Hwang; Ji Eun Choi; Anna Cho; Jangsup Moon; Moon Woo Seong; Sung Sup Park; Yun Jeong Lee; Young Ok Kim; Jon Soo Kim; Won Seop Kim; Young Se Kwon; June Dong Park; Younjhin Ahn; Joo-Yeon Hwang; Hyun-Young Park; Youngha Lee; Murim Choi; Jong-Hee Chae
Journal:  Orphanet J Rare Dis       Date:  2019-03-20       Impact factor: 4.123

Review 5.  The Increasing Impact of Translational Research in the Molecular Diagnostics of Neuromuscular Diseases.

Authors:  Dèlia Yubero; Daniel Natera-de Benito; Jordi Pijuan; Judith Armstrong; Loreto Martorell; Guerau Fernàndez; Joan Maynou; Cristina Jou; Mònica Roldan; Carlos Ortez; Andrés Nascimento; Janet Hoenicka; Francesc Palau
Journal:  Int J Mol Sci       Date:  2021-04-20       Impact factor: 5.923

6.  Diagnostic odyssey of acute disseminated encephalomyelitis in children.

Authors:  Yoko Takahashi; Itaru Hayakawa; Yuichi Abe
Journal:  Sci Rep       Date:  2021-11-09       Impact factor: 4.379

7.  The diagnostic journey of genetically defined neurodevelopmental disorders.

Authors:  Juliana Simon; Carly Hyde; Vidya Saravanapandian; Rujuta Wilson; Charlotte Distefano; Aaron Besterman; Shafali Jeste
Journal:  J Neurodev Disord       Date:  2022-05-02       Impact factor: 4.074

8.  A Multi-Disciplinary Team Approach to Genomic Testing for Drug-Resistant Epilepsy Patients-The GENIE Study.

Authors:  Lata Vadlamudi; Carmen Maree Bennett; Melanie Tom; Ghusoon Abdulrasool; Kristian Brion; Ben Lundie; Hnin Aung; Chiyan Lau; Jonathan Rodgers; Kate Riney; Louisa Gordon
Journal:  J Clin Med       Date:  2022-07-21       Impact factor: 4.964

9.  Genome-Wide Sequencing for Unexplained Developmental Disabilities or Multiple Congenital Anomalies: A Health Technology Assessment.

Authors: 
Journal:  Ont Health Technol Assess Ser       Date:  2020-03-06

10.  Disclosure of genetic information to family members: a systematic review of normative documents.

Authors:  Amicia Phillips; Pascal Borry; Ine Van Hoyweghen; Danya F Vears
Journal:  Genet Med       Date:  2021-07-07       Impact factor: 8.822

  10 in total

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