Literature DB >> 29214564

Undiagnosed Diseases: Italy-US Collaboration and International Efforts to Tackle Rare and Common Diseases Lacking a Diagnosis.

Domenica Taruscio1, Giovanna Floridia2,3, Marco Salvatore2, Stephen C Groft4, William A Gahl5,6.   

Abstract

Rare diseases (RD), according to European Union criteria, affect 5 per 10,000 persons, or 30 million people, in the EU; in the USA, RD are defined as conditions that affect fewer than 200,000 individuals in the population (320 million). Most known rare disorders are severe and chronic, with many being degenerative and life threatening. There are roughly 5000-8000 rare diseases (European Commission, DG Health and Food Safety, Public Health, Rare Diseases, Policy.http://ec.europa.eu/health/rare_diseases/policy/index_en.htm. Accessed 19 December 2016; NORD-The National Organization for Rare Diseases: https://rarediseases.org/). Patient populations for individual RD are small and scattered; international collaborations are crucial to pool resources fragmented across individual countries for better diagnosis and treatment. Undiagnosed RD (URD) are conditions that elude diagnosis; some patients wait years for a definitive diagnosis. URD may include groups of unnamed disorders with common characteristics, phenotypically well described diseases, diseases with an unknown molecular basis, or those due to unknown, non-genetic factors.The US NIH Undiagnosed Diseases Program arose in 2008 to provide a diagnosis for individuals who had long sought one without success; in 2013 a nationwide Undiagnosed Diseases Network was established in the United States. In 2015, the Undiagnosed Disease Network International (UDNI) was established and includes US, Australia, Canada, Japan, Italy and other European countries. Other national initiatives have also been undertaken and are in progress all over the world.

Entities:  

Keywords:  Databases; Initiatives; Networks; Platforms; Programs; Undiagnosed diseases

Mesh:

Year:  2017        PMID: 29214564     DOI: 10.1007/978-3-319-67144-4_2

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN: 0065-2598            Impact factor:   2.622


  9 in total

1.  Rare disease care pathways in the EU: from odysseys and labyrinths towards highways.

Authors:  Birute Tumiene; Holm Graessner
Journal:  J Community Genet       Date:  2021-03-18

Review 2.  The case for open science: rare diseases.

Authors:  Yaffa R Rubinstein; Peter N Robinson; William A Gahl; Paul Avillach; Gareth Baynam; Helene Cederroth; Rebecca M Goodwin; Stephen C Groft; Mats G Hansson; Nomi L Harris; Vojtech Huser; Deborah Mascalzoni; Julie A McMurry; Matthew Might; Christoffer Nellaker; Barend Mons; Dina N Paltoo; Jonathan Pevsner; Manuel Posada; Alison P Rockett-Frase; Marco Roos; Tamar B Rubinstein; Domenica Taruscio; Esther van Enckevort; Melissa A Haendel
Journal:  JAMIA Open       Date:  2020-09-11

3.  SpainUDP: The Spanish Undiagnosed Rare Diseases Program.

Authors:  Estrella López-Martín; Beatriz Martínez-Delgado; Eva Bermejo-Sánchez; Javier Alonso; Manuel Posada
Journal:  Int J Environ Res Public Health       Date:  2018-08-14       Impact factor: 3.390

4.  Clinical utility in infants with suspected monogenic conditions through next-generation sequencing.

Authors:  Sha Hong; Li Wang; Dongying Zhao; Yonghong Zhang; Yan Chen; Jintong Tan; Lili Liang; Tianwen Zhu
Journal:  Mol Genet Genomic Med       Date:  2019-04-09       Impact factor: 2.183

5.  Evaluation of a clinical decision support system for rare diseases: a qualitative study.

Authors:  Jannik Schaaf; Martin Sedlmayr; Brita Sedlmayr; Hans-Ulrich Prokosch; Holger Storf
Journal:  BMC Med Inform Decis Mak       Date:  2021-02-18       Impact factor: 2.796

6.  Improving diagnosis for rare diseases: the experience of the Italian undiagnosed Rare diseases network.

Authors:  Marco Salvatore; Agata Polizzi; Maria Chiara De Stefano; Giovanna Floridia; Simone Baldovino; Dario Roccatello; Savino Sciascia; Elisa Menegatti; Giuseppe Remuzzi; Erica Daina; Paraskevas Iatropoulos; Bruno Bembi; Rosalia Maria Da Riol; Alessandra Ferlini; Marcella Neri; Giuseppe Novelli; Federica Sangiuolo; Francesco Brancati; Domenica Taruscio
Journal:  Ital J Pediatr       Date:  2020-09-14       Impact factor: 2.638

Review 7.  Meeting Patients' Right to the Correct Diagnosis: Ongoing International Initiatives on Undiagnosed Rare Diseases and Ethical and Social Issues.

Authors:  Sabina Gainotti; Deborah Mascalzoni; Virginie Bros-Facer; Carlo Petrini; Giovanna Floridia; Marco Roos; Marco Salvatore; Domenica Taruscio
Journal:  Int J Environ Res Public Health       Date:  2018-09-21       Impact factor: 3.390

Review 8.  Diagnosis of Rare Diseases: a scoping review of clinical decision support systems.

Authors:  Jannik Schaaf; Martin Sedlmayr; Johanna Schaefer; Holger Storf
Journal:  Orphanet J Rare Dis       Date:  2020-09-24       Impact factor: 4.123

9.  Interviews with experts in rare diseases for the development of clinical decision support system software - a qualitative study.

Authors:  Jannik Schaaf; Hans-Ulrich Prokosch; Martin Boeker; Johanna Schaefer; Jessica Vasseur; Holger Storf; Martin Sedlmayr
Journal:  BMC Med Inform Decis Mak       Date:  2020-09-16       Impact factor: 2.796

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.