An online compendium of treatable genetic disorders

被引:35
作者
Bick, David [1 ]
Bick, Sarah L. [2 ]
Dimmock, David P. [3 ]
Fowler, Tom A. [4 ,5 ]
Caulfield, Mark J. [4 ,5 ]
Scott, Richard H. [4 ,6 ]
机构
[1] HudsonAlpha Inst Biotechnol, Huntsville, AL 35806 USA
[2] Nemours Alfred I DuPont Hosp Children, Wilmington, DE USA
[3] Rady Childrens Inst Genom Med, San Diego, CA USA
[4] Genom England Ltd, London, England
[5] Queen Mary Univ London, William Harvey Res Inst, London, England
[6] Great Ormond St Hosp Children Natl Hlth Serv NHS, Dept Clin Genet, London, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
genetic diseases; internet; mobile application; treatment;
D O I
10.1002/ajmg.c.31874
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
More than 4,000 genes have been associated with recognizable Mendelian/monogenic diseases. When faced with a new diagnosis of a rare genetic disorder, health care providers increasingly turn to internet resources for information to understand the disease and direct care. Unfortunately, it can be challenging to find information concerning treatment for rare diseases as key details are scattered across a number of authoritative websites and numerous journal articles. The website and associated mobile device application described in this article begin to address this challenge by providing a convenient, readily available starting point to find treatment information. The site, (), is focused on those conditions where the treatment is directed against the mechanism of the disease and thereby alters the natural history of the disease. The website currently contains 633 disease entries that include references to disease information and treatment guidance, a brief summary of treatments, the inheritance pattern, a disease frequency (if known), nonmolecular confirmatory testing (if available), and a link to experimental treatments. Existing entries are continuously updated, and new entries are added as novel treatments appear in the literature.
引用
收藏
页码:48 / 54
页数:7
相关论文
共 27 条
[1]   The role of exome sequencing in newborn screening for inborn errors of metabolism [J].
Adhikari, Aashish N. ;
Gallagher, Renata C. ;
Wang, Yaqiong ;
Currier, Robert J. ;
Amatuni, George ;
Bassaganyas, Laia ;
Chen, Flavia ;
Kundu, Kunal ;
Kvale, Mark ;
Mooney, Sean D. ;
Nussbaum, Robert L. ;
Randi, Savanna S. ;
Sanford, Jeremy ;
Shieh, Joseph T. ;
Srinivasan, Rajgopal ;
Sunderam, Uma ;
Tang, Hao ;
Vaka, Dedeepya ;
Zou, Yangyun ;
Koenig, Barbara A. ;
Kwok, Pui-Yan ;
Risch, Neil ;
Puck, Jennifer M. ;
Brenner, Steven E. .
NATURE MEDICINE, 2020, 26 (09) :1392-1397
[2]   International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases [J].
Boycott, Kym M. ;
Rath, Ana ;
Chong, Jessica X. ;
Hartley, Taila ;
Alkuraya, Fowzan S. ;
Baynam, Gareth ;
Brookes, Anthony J. ;
Brudno, Michael ;
Carracedo, Angel ;
den Dunnen, Johan T. ;
Dyke, Stephanie O. M. ;
Estivill, Xavier ;
Goldblatt, Jack ;
Gonthier, Catherine ;
Groft, Stephen C. ;
Gut, Ivo ;
Hamosh, Ada ;
Hieter, Philip ;
Hoehn, Sophie ;
Hurles, Matthew E. ;
Kaufmann, Petra ;
Knoppers, Bartha M. ;
Krischer, Jeffrey P. ;
Macek, Milan, Jr. ;
Matthijs, Gert ;
Olry, Annie ;
Parker, Samantha ;
Paschall, Justin ;
Philippakis, Anthony A. ;
Rehm, Heidi L. ;
Robinson, Peter N. ;
Sham, Pak-Chung ;
Stefanov, Rumen ;
Taruscio, Domenica ;
Unni, Divya ;
Vanstone, Megan R. ;
Zhang, Feng ;
Brunner, Han ;
Bamshad, Michael J. ;
Lochmueller, Hanns .
AMERICAN JOURNAL OF HUMAN GENETICS, 2017, 100 (05) :695-705
[3]  
Brugada R., 2016, BRUGADA SYNDROME GEN, P1993
[4]   Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project [J].
Ceyhan-Birsoy, Ozge ;
Murry, Jaclyn B. ;
Machini, Kalotina ;
Lebo, Matthew S. ;
Yu, Timothy W. ;
Fayer, Shawn ;
Genetti, Casie A. ;
Schwartz, Talia S. ;
Agrawal, Pankaj B. ;
Parad, Richard B. ;
Holm, Ingrid A. ;
McGuire, Amy L. ;
Green, Robert C. ;
Rehm, Heidi L. ;
Beggs, Alan H. ;
Betting, Wendi N. ;
Christensen, Kurt D. ;
Dukhovny, Dmitry ;
Frankel, Leslie A. ;
Graham, Chet ;
Guiterrez, Amanda M. ;
Harden, Maegan ;
Krier, Joel B. ;
Levy, Harvey L. ;
Lu, Xingquan ;
Naik, Medha ;
Nguyen, Tiffany T. ;
Peoples, Hayley A. ;
Pereira, Stacey ;
Petersen, Devan ;
Ramamurthy, Uma ;
Ramanathan, Vivek ;
Roberts, Amy ;
Robinson, Jill O. ;
Roumiantsev, Serguei ;
Truong, Tina K. ;
Vannoy, Grace E. ;
Waisbren, Susan E. .
AMERICAN JOURNAL OF HUMAN GENETICS, 2019, 104 (01) :76-93
[5]   Should states adopt newborn screening for early infantile Krabbe disease? [J].
Dimmock, David P. .
GENETICS IN MEDICINE, 2016, 18 (03) :217-220
[6]  
Eng C., 2019, MULTIPLE ENDOCRINE N, P1993
[7]   How genomic information is accessed in clinical practice: an electronic survey of UK general practitioners [J].
Evans, W. R. H. ;
Tranter, J. ;
Rafi, I. ;
Hayward, J. ;
Qureshi, N. .
JOURNAL OF COMMUNITY GENETICS, 2020, 11 (03) :377-386
[8]   TQuest, A Web-Based Platform to Enable Precision Medicine by Linking a Tumor's Genetic Defects to Therapeutic Options [J].
Gershkovich, Peter ;
Platt, James ;
Knopf, Joshua ;
Tasoulis, Marios K. ;
Shi, Weiwei ;
Pusztai, Lajos ;
Hatzis, Christos .
JCO CLINICAL CANCER INFORMATICS, 2018, 2 :1-13
[9]   Dietary interventions for phenulketonuria [J].
Jameson, Elisabeth ;
Remmington, Tracey .
COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2020, (07)
[10]  
Katsoulakis E., 2020, JCO PRECIS ONCOL, V4, DOI [10.1200/PO.19.00118, DOI 10.1200/P0.19.00118]