Literature DB >> 27894438

How Doctors Think: Common Diagnostic Errors in Clinical Judgment-Lessons from an Undiagnosed and Rare Disease Program.

Robert M Kliegman1, Brett J Bordini2, Donald Basel2, James J Nocton2.   

Abstract

The scientific process of analysis and deduction is frequently, often subconsciously, used by physicians to develop a differential diagnosis based on patients' symptoms. Common disorders are most frequently diagnosed in general practice. Rare diseases are uncommon and frequently remain undiagnosed for many years. Cognitive errors in clinical judgment delay definitive diagnosis. Whole-exome sequencing has helped identify the cause of undiagnosed or rare diseases in up to 40% of children. This article provides experiences with an undiagnosed or rare disease program, where detailed data accumulation and a multifaceted analytical approach assisted in diagnosing atypical presentations of common disorders. Copyright Â
© 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Misdiagnosis; Undiagnosed or rare diseases (URDs); Whole-exome sequencing

Mesh:

Year:  2017        PMID: 27894438     DOI: 10.1016/j.pcl.2016.08.002

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


  5 in total

Review 1.  Estimating the number of diseases - the concept of rare, ultra-rare, and hyper-rare.

Authors:  C I Edvard Smith; Peter Bergman; Daniel W Hagey
Journal:  iScience       Date:  2022-07-01

Review 2.  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

3.  Training Internal Medicine Residents in Difficult Diagnosis: A Novel Diagnostic Second Opinion Clinic Experience.

Authors:  Stefano Testa; Mugdha Joshi; Justin Lotfi; Bryant Lin; Maja Artandi; Kim F Chiang; Kevin Chang; Baldeep Singh; Linda N Geng
Journal:  J Med Educ Curric Dev       Date:  2022-03-29

4.  Misdiagnosis of trisomy 13 and trisomy 18 is more common than anticipated.

Authors:  Gabrielle C Geddes; Niloufar Hafezi; Brian W Gray
Journal:  Am J Med Genet A       Date:  2022-08-04       Impact factor: 2.578

5.  Validation of a computational phenotype for finding patients eligible for genetic testing for pathogenic PTEN variants across three centers.

Authors:  Cartik Kothari; Siddharth Srivastava; Youssef Kousa; Rima Izem; Marcin Gierdalski; Dongkyu Kim; Amy Good; Kira A Dies; Gregory Geisel; Hiroki Morizono; Vittorio Gallo; Scott L Pomeroy; Gwenn A Garden; Lisa Guay-Woodford; Mustafa Sahin; Paul Avillach
Journal:  J Neurodev Disord       Date:  2022-03-23       Impact factor: 4.025

  5 in total

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