Ldrtc Is A Non Profit Organization Founded In 2013 By Drozlem Goker Alpan With A Vision To Provide High Quality Care For Individuals With Lysosomal Storage Diseases And Other Rare Genetic Disordersdrozlem Goker Alpan Is A World Renowned Authority In The Field Of Lysosomal And Other Rare Genetic Disorders And Is Well Known For Her Dedication To The Health And Well Being Of Her Patients And Families Our Goal Ldrtc Utilizes A Variety Of Clinical Treatment And Research Protocolsconducts Training Programs To Increase Awarenessand Offers Compassionate Care And A Platform For The Patients And Families Affected By These Debilitating Disordersour Commitment Research To Unravel Underlying Disease Causing Mechanismsdiscover New Biomarkersand Explore New Therapeutic Pathways And Treatment Options Education For Patientsfamilieshealthcare Providersand Researchers In The Fieldtreatment And Clinical Care For Persons Suffering From Lysosomal And Other Rare Diseases Our Approach Ldrtc Aims To Bridge The Gap Between Basic And Clinical Research To Facilitate The Diagnosistreatmentand Management Of Rare Disordersldrtc Presents A Unique Translational Research Model Focusing On Amultidisciplinary Approach To Study The Disease Pathology While Applying Cellularmolecular And Immunologic Concepts To Pathways Amenable To Therapeutic Modulationour Goal Is To Implement Personalized Medicine Wherein We Recognize And Acknowledge Unique Medical Histories Presented By Individuals With Rare Disorders And Ultimately Offer Medical Carewe Believe Novel Treatment Options Are Worth Exploring Even If They Benefit As Few As A Single Patientwe Design And Offer Truebench To Bedsideclinical Protocols Where There Is A Need To Study A Disease Aspect Or A Mechanism For Which There Is An Already Existing Therapydrug Re Purposingor A Pipeline Product
