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dystrophy

Synonyms

Noun

1. muscular dystrophy

2. genetic disease, genetic disorder, genetic abnormality, genetic defect, congenital disease, inherited disease, inherited disorder, hereditary disease, hereditary condition, degenerative disorder

Usage
FDA Accepts Sarepta's sNDAs for Casimersen and Golodirsen for Duchenne Muscular Dystrophy - NeurologyLive
Treating Duchenne muscular dystrophy before symptoms emerge may improve motor function, clinical trial suggests - Medical Xpress
Anesthetic Management of a 33-Year-Old Female With Limb-Girdle Muscular Dystrophy Undergoing Laparoscopic Cholecystectomy: A Case Report - Cureus
Epicrispr gene silencer enhances muscle in muscular dystrophy - Fierce Biotech
Burn Boot Camp and Muscular Dystrophy Association Raise - GlobeNewswire
SonoThera Targets 2027 for First Clinical Trial of Duchenne Gene Therapy - Precision Medicine Online
Sarepta Moves Closer To FDA Approval For Duchenne Muscular Dystrophy Drugs - Benzinga
Novel gene therapy platform restores muscle function in models of Duchenne muscular dystrophy - UT MD Anderson
Wellstone Muscular Dystrophy Cooperative Research Center - UT Southwestern Medical Center
Meta-Analysis Evaluates Duchenne Muscular Dystrophy Treatments’ Safety - Bioengineer.org
FDA Advisory Committee Schedules Meeting to Review Deramiocel's BLA in Duchenne Muscular Dystrophy - NeurologyLive
Unlocking new paths in muscular dystrophy treatment - University of Nevada, Reno
FDA grants GEn-1123 rare disease designations for Duchenne muscular dystrophy - Contemporary Pediatrics
Acquisition of Edgewise Therapeutics’ Muscular Dystrophy Business - Servier
Family of drugs used for treating muscular dystrophy could improve brain tumor treatment - Medical Xpress
An Antibody–Oligonucleotide Conjugate for Myotonic Dystrophy Type 1 - The New England Journal of Medicine
Impaired stem cell migration and divisions in Duchenne muscular dystrophy revealed by live imaging - Nature
Santhera Notes Topline Results from Catalyst Pharmaceuticals’ Phase 1 Clinical Study of AGAMREE® - GlobeNewswire
Capricor Therapeutics Announces FDA Advisory Committee - GlobeNewswire
Top 10 muscular dystrophy news stories of 2025 - Muscular Dystrophy News
Toward Trial Readiness in Congenital Myotonic Dystrophy - Neurology® Journals
Capricor thrown for another loop as FDA sets adcomm for DMD cardiomyopathy therapy - BioSpace
Interpreting Long-Term MESA Data of Sevasemten to Treat Becker Muscular Dystrophy - NeurologyLive
Capricor to Present Positive Five-Year HOPE-2 OLE Data and - GlobeNewswire
Source of gastrointestinal problems in myotonic dystrophy - National Institutes of Health (NIH) | (.gov)
Phase 3 HOPE-3 Data Reinforce Skeletal and Cardiac Benefits of Deramiocel in Duchenne Muscular Dystrophy - CGTLive®
Elixirgen and Nippon Shinyaku sign EXG-7001 option agreement - BioWorld News
MDA pushes back on DOJ memorandum about disability care - Muscular Dystrophy News
Real-world experience with gene therapy in Duchenne muscular dystrophy center readiness and patients safety: report from Qatar - Nature
Broken William Ziegler Elementary School elevator forces student with muscular dystrophy to climb stairs for weeks - 6abc Philadelphia
FDA accepts BridgeBio’s application for potential first limb-girdle muscular dystrophy drug - BioSpace
Sevasemten’s Effect on Cardiovascular Markers Indicate Protective Role in Becker Muscular Dystrophy - NeurologyLive
Design Therapeutics Announces Initiation of Patient Dosing in Phase 1 Multiple Ascending Dose Trial of DT-818 for Myotonic Dystrophy Type-1 - The Manila Times
Servier inks $2.6B buyout of Edgewise’s muscular dystrophy unit to beef up neurology pipeline - Fierce Biotech
RNA Toxicity Is a Driver of Heart Disease in Muscular Dystrophy - Inside Precision Medicine
Novartis' phase 1/2 win tees up regulatory talks about dystrophy drug from $12B Avidity takeover - Fierce Biotech
Quantitative 3D assessment of muscle dystrophy through X-ray phase-contrast tomography - Nature
New treatments available for Duchenne Muscular Dystrophy - KPLC 7 News
Development of a cost-effectiveness analysis model for Duchenne muscular dystrophy utilizing the national registry in Japan - Nature
Canadian fire fighters raise $1.1 million for Muscular Dystrophy Canada - IAFF
Muscular Dystrophy Association Names Pamela Kournetas as Chief Financial Officer - Muscular Dystrophy Association
SEEN: All That Jazz 2026 - Times Union
Servier frees Edgewise for cardio mission with $2.65B muscular dystrophy deal - BioSpace
VCU Health launches nation’s first LGMD Center of Excellence - VCU Health
HDAC11 protein identified as potential target for Duchenne muscular dystrophy - Drug Target Review
Belle Plaine boy with muscular dystrophy plays vital role on baseball team - CBS News
Myotonic dystrophy type 1: clinical diversity, molecular insights and therapeutic perspectives - Nature
Stanford students work toward cure for rare muscular dystrophy - Stanford Report
Expert Consensus on Genetic Diagnostic Approaches for Patients With Limb-Girdle Muscular Dystrophy - Neurology® Journals
PepGen muscular dystrophy drug gets ‘surprise’ hold from FDA - BioPharma Dive
Clarity at Last: Moving Forward with a Limb-Girdle Muscular Dystrophy Diagnosis - Brain & Life
Sarepta Provides Progress Update for SRP-1003, its Investigational siRNA treatment for Myotonic Dystrophy Type 1 - Sarepta Therapeutics
VCU and UAlbany earn $6.5M grant to launch a Wellstone muscular dystrophy center - VCU News
Upper limb function and quality of life in Duchenne muscular dystrophy: a cross-sectional study in Chile - Nature
Fishing for novel HDAC inhibitor compounds to treat Duchenne muscular dystrophy - ScienceDirect.com
Capricor's Duchenne drug shows 5-year muscle and heart data at PPMD - Stock Titan
Muscular Dystrophy Association to Honor UNLV’s Łukasz Sznajder with Inaugural Research Momentum Award - University of Nevada, Las Vegas | UNLV
Breakthroughs in treatment offer hope for rare Duchenne muscular dystrophy - WISH-TV
Muscular Dystrophy Association Announces $100,000 Investment to Advance LGMD Care at Leading MDA Care Centers with BridgeBio - Muscular Dystrophy Association
A Decade of Strength: Muscular Dystrophy Association and Burn Boot Camp Team Up for 10th Annual ‘Be Their Muscle’ Campaign - Muscular Dystrophy Association
A new biomarker for a form of muscular dystrophy could improve disease monitoring in patients - Fred Hutchinson Cancer Center
Senator Collins Recognized by Parent Project Muscular Dystrophy - U.S. Senator Susan Collins (.gov)
Organizations Join Forces to Map How Human Muscle Regenerates - Muscular Dystrophy Association
Servier Moves Into Muscular Dystrophy, Paying $1.5B for Assets From Edgewise Therapeutics - MedCity News
Sarepta CEO Doug Ingram To Step Down as Muscular Dystrophy Mission Hits Home - BioSpace
Diversity challenges and reconciles genetics in facioscapulohumeral muscular dystrophy - Nature
Researchers provide answers to progressive heart problems in muscular dystrophy and potential reversibility - Baylor College of Medicine Blog Network -
After Toddler's Wheelchair Grew Too Heavy to Carry Up the Stairs, Parents Installed an Elevator in Their Residential Home (Exclusive) - People.com
Muscular Dystrophy Association Announces nearly $2 Million in Collaborative Research Grants Advancing Treatments Across Multiple Neuromuscular Diseases - Muscular Dystrophy Association
Muscular Dystrophy Association Marks Rare Disease Day by Spotlighting Community Stories Driving Progress in Research, Care, and Advocacy - Muscular Dystrophy Association
Neonatal congenital myotonic dystrophy with DMPK gene expansion: clinical features and short-term outcomes - Frontiers
New era for fighting rare childhood disease: Duchenne Muscular Dystrophy - News4JAX
Muscular Dystrophy Association Welcomes Amanda Baze Hall to Board of Directors - Muscular Dystrophy Association
Cell Therapy Slows Upper Limb Decline in Duchenne Muscular Dystrophy - MedPage Today
Disease Progression and Quality of Life in Duchenne Muscular Dystrophy - NeurologyLive
Neurofilament light chain reflects motor impairment in myotonic dystrophy type 1 - Frontiers
Elixirgen Therapeutics And Nippon Shinyaku Enter Into An Option Agreement For The Development And Commercialization Of Exg-7001 For Duchenne Muscular Dystrophy - TradingView
Science & Medicine: Why are neurodevelopmental disorders common in Duchenne muscular dystrophy? - Texas Public Radio | TPR
World Duchenne Awareness Day 7 September - Welcome to the United Nations
Duchenne Muscular Dystrophy Clinical Trial Pipeline: DelveInsight Highlights Major Advances, Transformative Therapies, and 75+ Leading Players Wheeling the Therapeutics Landscape - GlobeNewswire
Dad 'incredibly happy' that son can access new drug - BBC
Muscular Dystrophy Association Honors National Family Caregivers Month with Advocacy and Awareness Nationwide - Muscular Dystrophy Association
I’m conflicted about the idea of a cure for muscular dystrophy - Muscular Dystrophy News
Morrison champions resolution declaring September 2026 Muscular Dystrophy Awareness Month - Illinois Senate Democratic Caucus
Groundbreaking treatment for local boy with Duchenne Muscular Dystrophy - kobi5.com
Muscular Dystrophy Association Names Sharon Hesterlee, PhD, as President and Chief Executive Officer - Muscular Dystrophy Association
BridgeBio Builds Case for Early 2027 Launch of Dystrophy Drug - BioSpace
Canadian affiliates recognized by Muscular Dystrophy Canada - IAFF
Antibody-Oligonucleotide Conjugate Shows Promise in Myotonic Dystrophy Type 1 - MedPage Today
Gene Therapy for Duchenne Muscular Dystrophy: Genethon Confirms Two-Year Efficacy in Patients Treated with Its Drug Candidate GNT0004 at Therapeutic Dose in the First Phase of Its Clinical Trial - BioSpace
Current Trends in Duchenne Muscular Dystrophy Research and Therapy: 3D Cardiac Modelling - Wiley Online Library
An antibody-siRNA conjugate could treat myotonic dystrophy - BioXconomy
Sensorion axes hearing loss program; Novartis’ biomarker data in muscular dystrophy - Endpoints News
7 Tips for Boosting Energy With Duchenne Muscular Dystrophy - Everyday Health
Assessing Delays in Time to Diagnosis of Duchenne Muscular Dystrophy: A Survey of Current Primary Care Practices - Cureus
CSF Proteomic Profiling Reveals Altered Pathways in Myotonic Dystrophy Type 1 (P2-11.029) - Neurology® Journals
Iron supplements restore muscle strength in mouse model of muscular dystrophy - Medical Xpress
The life with Duchenne muscular dystrophy no one said I could live - Muscular Dystrophy News
CDC is Making a Difference for People with Muscular Dystrophy - Centers for Disease Control and Prevention | CDC (.gov)
Epicrispr Reports First Clinical Evidence of Increased Lean Muscle Volume in Patients with FSHD Following Treatment with EPI-321 - Business Wire
Foreign Language Equivalents
Foreign Language Equivalents of 'dystrophy'
Language Equivalent   Language Equivalent
French    Spanish
Misspellings - Typos
dtstrophy,   dystrpohy,   dystrophhy,   dystro[hy,   dystropy,   dystroophy,   dystroph,   dystropphy,   ystrophy,   dystrphy,   dystrpphy,   dysstrophy,   dystrophyy,   dysttrophy,   dystorphy,   dyystrophy,   dytrophy,   dystrophu,   dysrophy,   dytsrophy,   dystriphy,   ydstrophy,   dystrohpy,   fystrophy,   dustrophy,   dysrtophy,   dystropgy,   dstrophy,   dsytrophy,   dystroohy,   dystropjy,   dystropyh,   dysteophy,   dydtrophy,   dystrohy,   dyatrophy,   dystropht,   dysyrophy,   dystophy,   dysttophy,   dysrrophy,   ddystrophy,   dystrrophy,   systrophy
Words Starting with Letter - 'A'
a a battery a billion
a bit a bit much a capella singing
a cappella singing a couple of a few
a fortiori a good deal a great deal
a horizon a hundred a hundred and one
a hundred thousand a hundred times a kempis
a la carte a la mode a level
a little a lot a million
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