Literature DB >> 29325986

The Challenge of Rare Diseases.

James K Stoller1.   

Abstract

Rare diseases pose particular challenges to patients who are affected, to the clinicians who care for them, and to the investigators who study their conditions. Although individually uncommon, rare diseases are common in the aggregate, with approximately 7,000 described rare diseases affecting 25 to 30 million US adults. Challenges posed to affected individuals and their families largely regard being diagnosed, receiving optimal care, and affording disease-specific medications. Challenges facing clinicians who care for affected individuals include gaining knowledge and experience in caring for such patients, and the availability of local experts and of expert guidelines. Finally, challenges to investigators regard the difficulty and expense of assembling large cohorts of affected individuals for study, and garnering funding for research. Fortunately, in the face of these challenges, the steadfast resolve of patient and clinical/scientific communities to enhance care and generate new knowledge has fostered a large inventory of countermeasures to offset these challenges. Although further progress is surely needed, successes to date include the formation of powerful patient advocacy groups which have brokered collaborations between the patient, scientific communities, the government, and pharma/device communities in service of detection, optimal care, and research; procurement of funds to support research; formation of consortia of clinicians and scientists to collaborate; and general activation of the respective patient communities to perpetuate these successes. Persisting needs include enhanced detection strategies, dissemination of knowledge regarding optimal care, and research to prevent, treat, and cure disease.
Copyright © 2018 American College of Chest Physicians. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  alpha-1 antitrypsin deficiency; lymphangioleiomyomatosis; rare disease

Mesh:

Year:  2018        PMID: 29325986     DOI: 10.1016/j.chest.2017.12.018

Source DB:  PubMed          Journal:  Chest        ISSN: 0012-3692            Impact factor:   9.410


  24 in total

Review 1.  Next Generation Sequencing and Bioinformatics Analysis of Family Genetic Inheritance.

Authors:  Aquillah M Kanzi; James Emmanuel San; Benjamin Chimukangara; Eduan Wilkinson; Maryam Fish; Veron Ramsuran; Tulio de Oliveira
Journal:  Front Genet       Date:  2020-10-23       Impact factor: 4.599

Review 2.  Therapeutic landscape for Batten disease: current treatments and future prospects.

Authors:  Tyler B Johnson; Jacob T Cain; Katherine A White; Denia Ramirez-Montealegre; David A Pearce; Jill M Weimer
Journal:  Nat Rev Neurol       Date:  2019-03       Impact factor: 42.937

3.  Willingness of patients with sarcoma to participate in cancer surveillance research: a cross-sectional patient survey.

Authors:  Patricia Schneider; Victoria Giglio; Dana Ghanem; David Wilson; Robert Turcotte; Marc Isler; Sophie Mottard; Benjamin Miller; James Hayden; Yee-Cheen Doung; Kenneth Gundle; R Lor Randall; Kevin Jones; Roberto Vélez; Michelle Ghert
Journal:  BMJ Open       Date:  2021-02-26       Impact factor: 2.692

4.  Genomic test ends a long diagnostic odyssey in a patient with resistance to thyroid hormones.

Authors:  Carola G Vinuesa; Olivija Vaskova; Todor Arsov; Chengmei Xie; Nan Shen; Dan Andrews
Journal:  Thyroid Res       Date:  2019-07-15

5.  The Caregiving Experiences of Fathers and Mothers of Children With Rare Diseases in Italy: Challenges and Social Support Perceptions.

Authors:  Paola Cardinali; Laura Migliorini; Nadia Rania
Journal:  Front Psychol       Date:  2019-08-05

Review 6.  Outcomes in pediatric studies of medium-chain acyl-coA dehydrogenase (MCAD) deficiency and phenylketonuria (PKU): a review.

Authors:  Michael Pugliese; Kylie Tingley; Andrea Chow; Nicole Pallone; Maureen Smith; Alvi Rahman; Pranesh Chakraborty; Michael T Geraghty; Julie Irwin; Laure Tessier; Stuart G Nicholls; Martin Offringa; Nancy J Butcher; Ryan Iverson; Tammy J Clifford; Sylvia Stockler; Brian Hutton; Karen Paik; Jessica Tao; Becky Skidmore; Doug Coyle; Kathleen Duddy; Sarah Dyack; Cheryl R Greenberg; Shailly Jain Ghai; Natalya Karp; Lawrence Korngut; Jonathan Kronick; Alex MacKenzie; Jennifer MacKenzie; Bruno Maranda; John J Mitchell; Murray Potter; Chitra Prasad; Andreas Schulze; Rebecca Sparkes; Monica Taljaard; Yannis Trakadis; Jagdeep Walia; Beth K Potter
Journal:  Orphanet J Rare Dis       Date:  2020-01-14       Impact factor: 4.123

7.  Opportunities and pitfalls of social media research in rare genetic diseases: a systematic review.

Authors:  Emily G Miller; Amanda L Woodward; Grace Flinchum; Jennifer L Young; Holly K Tabor; Meghan C Halley
Journal:  Genet Med       Date:  2021-07-19       Impact factor: 8.864

Review 8.  Establishing Patient Registries for Rare Diseases: Rationale and Challenges.

Authors:  Vanessa Boulanger; Marissa Schlemmer; Suzanne Rossov; Allison Seebald; Pamela Gavin
Journal:  Pharmaceut Med       Date:  2020-06

Review 9.  Succinic Semialdehyde Dehydrogenase Deficiency: An Update.

Authors:  Miroslava Didiášová; Antje Banning; Heiko Brennenstuhl; Sabine Jung-Klawitter; Claudio Cinquemani; Thomas Opladen; Ritva Tikkanen
Journal:  Cells       Date:  2020-02-19       Impact factor: 6.600

Review 10.  Artificial Intelligence (AI) in Rare Diseases: Is the Future Brighter?

Authors:  Sandra Brasil; Carlota Pascoal; Rita Francisco; Vanessa Dos Reis Ferreira; Paula A Videira; And Gonçalo Valadão
Journal:  Genes (Basel)       Date:  2019-11-27       Impact factor: 4.096

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