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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
Colton friends hitting the trail to fight Muscular Dystrophy - Woodburn Independent
Binghamton University research study advances treatment for Duchenne muscular dystrophy - Binghamton University
FDA Accepts Sarepta's sNDAs for Casimersen and Golodirsen for Duchenne Muscular Dystrophy - NeurologyLive
Sarepta Announces FDA Acceptance of sNDAs for AMONDYS 45® and VYONDYS 53® - Sarepta Therapeutics
FDA review begins for full approval bids on 2 Duchenne therapies - Muscular Dystrophy News
Epicrispr gene silencer enhances muscle in muscular dystrophy - Fierce Biotech
Novel gene therapy platform restores muscle function in models of Duchenne muscular dystrophy - UT MD Anderson
Satellos Bioscience Fast Track Win Fuels DMD Hopes - Streetwise Reports
University of Florida lab uses MRI-based methods to track muscle injury and recovery - WCJB
Sarepta Moves Closer To FDA Approval For Duchenne Muscular Dystrophy Drugs - Benzinga
Family of drugs used for treating muscular dystrophy could improve brain tumor treatment - Medical Xpress
FDA grants GEn-1123 rare disease designations for Duchenne muscular dystrophy - Contemporary Pediatrics
SonoThera Targets 2027 for First Clinical Trial of Duchenne Gene Therapy - Precision Medicine Online
The search for better accommodations for my disease progression continues - Muscular Dystrophy News
Wellstone Muscular Dystrophy Cooperative Research Center - UT Southwestern
Acquisition of Edgewise Therapeutics’ Muscular Dystrophy Business - Servier
Novartis' phase 1/2 win tees up regulatory talks about dystrophy drug from $12B Avidity takeover - Fierce Biotech
July meeting date set for FDA, developer to talk deramiocel for DMD - Muscular Dystrophy News
Unlocking new paths in muscular dystrophy treatment - University of Nevada, Reno
Vamorolone for Duchenne Muscular Dystrophy - Neurology® Journals
After Toddler's Wheelchair Grew Too Heavy to Carry Up the Stairs, Parents Installed an Elevator in Their Residential Home (Exclusive) - People.com
Sensorion axes hearing loss program; Novartis’ biomarker data in muscular dystrophy - Endpoints News
Meta-Analysis Evaluates Duchenne Muscular Dystrophy Treatments’ Safety - Bioengineer.org
Phase 3 HOPE-3 Data Reinforce Skeletal and Cardiac Benefits of Deramiocel in Duchenne Muscular Dystrophy - CGTLive®
Servier inks $2.6B buyout of Edgewise’s muscular dystrophy unit to beef up neurology pipeline - Fierce Biotech
Toward Trial Readiness in Congenital Myotonic Dystrophy - Neurology® Journals
Interpreting Long-Term MESA Data of Sevasemten to Treat Becker Muscular Dystrophy - NeurologyLive
FDA accepts BridgeBio’s application for potential first limb-girdle muscular dystrophy drug - BioSpace
Broken William Ziegler Elementary School elevator forces student with muscular dystrophy to climb stairs for weeks - 6abc Philadelphia
Edgewise Therapeutics Reports First Quarter 2026 Financial Results and Advances Clinical Programs in Muscular Dystrophy and Cardiovascular Indications - PR Newswire
New treatments available for Duchenne Muscular Dystrophy - KPLC 7 News
Servier frees Edgewise for cardio mission with $2.65B muscular dystrophy deal - BioSpace
Canadian fire fighters raise $1.1 million for Muscular Dystrophy Canada - IAFF
RNA Toxicity Is a Driver of Heart Disease in Muscular Dystrophy - Inside Precision Medicine
New era for fighting rare childhood disease: Duchenne Muscular Dystrophy - News4JAX
Muscular Dystrophy Association Announces $100,000 Investment to Advance LGMD Care at Leading MDA Care Centers with BridgeBio - Muscular Dystrophy Association
Muscular Dystrophy Association Names Pamela Kournetas as Chief Financial Officer - Muscular Dystrophy Association
VCU Health launches nation’s first LGMD Center of Excellence - VCU Health
Sevasemten’s Effect on Cardiovascular Markers Indicate Protective Role in Becker Muscular Dystrophy - NeurologyLive
Clarity at Last: Moving Forward with a Limb-Girdle Muscular Dystrophy Diagnosis - Brain & Life
Servier Moves Into Muscular Dystrophy, Paying $1.5B for Assets From Edgewise Therapeutics - MedCity News
A Decade of Strength: Muscular Dystrophy Association and Burn Boot Camp Team Up for 10th Annual ‘Be Their Muscle’ Campaign - Muscular Dystrophy Association
Epicrispr Reports First Clinical Evidence of Increased Lean Muscle Volume in Patients with FSHD Following Treatment with EPI-321 - Business Wire
Impaired stem cell migration and divisions in Duchenne muscular dystrophy revealed by live imaging - Nature
Stanford students work toward cure for rare muscular dystrophy - Stanford Report
Duchenne Muscular Dystrophy Clinical Trial Pipeline: DelveInsight Highlights Major Advances, Transformative Therapies, and 75+ Leading Players Wheeling the Therapeutics Landscape - GlobeNewswire
A new biomarker for a form of muscular dystrophy could improve disease monitoring in patients - Fred Hutchinson Cancer Center
PepGen muscular dystrophy drug gets ‘surprise’ hold from FDA - BioPharma Dive
Cell Therapy Slows Upper Limb Decline in Duchenne Muscular Dystrophy - MedPage Today
Morrison champions resolution declaring September 2026 Muscular Dystrophy Awareness Month - Illinois Senate Democratic Caucus
Researchers provide answers to progressive heart problems in muscular dystrophy and potential reversibility - Baylor College of Medicine Blog Network -
Senator Collins Recognized by Parent Project Muscular Dystrophy - U.S. Senator Susan Collins (.gov)
Science & Medicine: Why are neurodevelopmental disorders common in Duchenne muscular dystrophy? - Texas Public Radio | TPR
Muscular Dystrophy Association to Honor UNLV’s Łukasz Sznajder with Inaugural Research Momentum Award - University of Nevada, Las Vegas | UNLV
7 Tips for Boosting Energy With Duchenne Muscular Dystrophy - Everyday Health
HDAC11 protein identified as potential target for Duchenne muscular dystrophy - Drug Target Review
Sarepta CEO Doug Ingram To Step Down as Muscular Dystrophy Mission Hits Home - BioSpace
How to Navigate School and Workplace Accommodations With Duchenne Muscular Dystrophy - Everyday Health
Parents of children with Duchenne muscular dystrophy expect a concrete decision on medication from the Prime - sovanews.tv
Muscular Dystrophy Association Welcomes Amanda Baze Hall to Board of Directors - Muscular Dystrophy Association
Servier to buy Edgewise’s muscular dystrophy biz in $2.65bn deal - BioXconomy
Euglycemic ketoacidosis in a nondiabetic patient with Duchenne muscular dystrophy on dapagliflozin: comment - Springer Nature Link
An antibody-siRNA conjugate could treat myotonic dystrophy - BioXconomy
BridgeBio Builds Case for Early 2027 Launch of Dystrophy Drug - BioSpace
Groundbreaking treatment for local boy with Duchenne Muscular Dystrophy - kobi5.com
Nonprofit aids mother whose son has Duchenne Muscular Dystrophy - WBAL-TV
Mother urges FDA chief to speed Duchenne muscular dystrophy treatments - KFOX
Antibody-Oligonucleotide Conjugate Shows Promise in Myotonic Dystrophy Type 1 - MedPage Today
Organizations Join Forces to Map How Human Muscle Regenerates - Muscular Dystrophy Association
Source of gastrointestinal problems in myotonic dystrophy - National Institutes of Health (NIH) | (.gov)
Man stops in Tampa before finishing 200k miles on motorcycle for rare disease - Spectrum Bay News 9
Solid Biosciences to Present at the 2026 Muscular Dystrophy Association (MDA) Clinical & Scientific Conference - Yahoo Finance
NHS access approved for new Duchenne muscular dystrophy treatment - National Health Executive
Muscular Dystrophy Association Marks Rare Disease Day by Spotlighting Community Stories Driving Progress in Research, Care, and Advocacy - Muscular Dystrophy Association
Muscular Dystrophy Association Announces Łukasz Sznajder, PhD, MSc, to Receive Inaugural MDA Research Momentum Award - Muscular Dystrophy Association
NICE approves Duchenne muscular dystrophy treatment givinostat after commercial deal sealed - Wired-Gov
Rally in Support of Children with Duchenne Muscular Dystrophy Held in Tbilisi - sovanews.tv
Iron supplements restore muscle strength in mouse model of muscular dystrophy - Medical Xpress
Myasthenia, SMA, Becker muscular dystrophy and GNE myopathy: Research highlights 2026 – No. 7 - afm-telethon.fr
Driven Coventry man to take on gruelling endurance challenges in memory of relatives - The Coventry Observer
Designer featured on Gardening Australia fears NDIA change a threat to his life - ABC News & Headlines – Australian Broadcasting Corporation
Students Raise 1 Mln in GEL for Children with Duchenne Dystrophy as Parents Fight for Modern Treatments - Civil Georgia
Research and Care Webinar: Spotlight on New Research - Muscular Dystrophy Association
Parents of Children with Duchenne Muscular Dystrophy hold March of Gratitude - 1TV.GE
Top 10 muscular dystrophy news stories of 2025 - Muscular Dystrophy News
Families of Children with Duchenne Muscular Dystrophy Demand Access to New Treatments, Meeting with Kobakhidze - Civil Georgia
Give your opinion on a genetically modified medicine against Duchenne Muscular Dystrophy - FPS Public Health
Neonatal congenital myotonic dystrophy with DMPK gene expansion: clinical features and short-term outcomes - Frontiers
Scientists apply genome editing to treat muscular dystrophy - 朝日新聞
Jet2 colleague raises over £2,000 for Muscular Dystrophy UK - Jet 2.com
Current Trends in Duchenne Muscular Dystrophy Research and Therapy: 3D Cardiac Modelling - Wiley Online Library
Applications Now Open for MDA’s 2026 Summer Camp Season - Muscular Dystrophy Association
Parents of children with Duchenne muscular dystrophy hold protest - 1TV.GE
Parents of children with Duchenne muscular dystrophy delivered their statement - 1TV.GE
Secretary Kennedy Adds Duchenne Muscular Dystrophy, Metachromatic Leukodystrophy to Newborn Screenings - HHS.gov
Real-world experience with gene therapy in Duchenne muscular dystrophy center readiness and patients safety: report from Qatar - Nature
Quantitative 3D assessment of muscle dystrophy through X-ray phase-contrast tomography - Nature
Expert Consensus on Genetic Diagnostic Approaches for Patients With Limb-Girdle Muscular Dystrophy - Neurology® Journals
Myotonic dystrophy type 1: clinical diversity, molecular insights and therapeutic perspectives - Nature
Development of a cost-effectiveness analysis model for Duchenne muscular dystrophy utilizing the national registry in Japan - Nature
Foreign Language Equivalents
Foreign Language Equivalents of 'dystrophy'
Language Equivalent   Language Equivalent
French    Spanish
Misspellings - Typos
dystophy,   dystropphy,   dyatrophy,   dystro[hy,   dystrophhy,   dsytrophy,   dystrophu,   dtstrophy,   dystropy,   ddystrophy,   dustrophy,   dystropyh,   dysyrophy,   dystroohy,   dystorphy,   dystropht,   dystropjy,   fystrophy,   dysteophy,   dysstrophy,   systrophy,   dystroophy,   dysrophy,   dytsrophy,   dysttophy,   dystrophyy,   dystrohpy,   dysrtophy,   dystrpphy,   dystrrophy,   dysrrophy,   dystropgy,   dstrophy,   ystrophy,   dystrohy,   dytrophy,   dystrpohy,   dysttrophy,   dystrphy,   dydtrophy,   dystriphy,   dystroph,   ydstrophy,   dyystrophy
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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