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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
Sarepta Announces FDA Acceptance of sNDAs for AMONDYS 45® and VYONDYS 53® - Sarepta Therapeutics
Binghamton University research study advances treatment for Duchenne muscular dystrophy - Binghamton University
Walk/roll through Maple Ridge park to find cure for Muscular Dystrophy - Maple Ridge News
CITGO Lemont Refinery raises $1.1 million for Muscular Dystrophy Association - Shaw Local
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
cTAP Announces Novel Prognostic Score Developed for Duchenne Muscular Dystrophy Patients Offers Improved Prediction of Loss of Ambulation - BioSpace
PARENTS TALK BACK From riding horses to power scooters - Daily American Republic
Vamorolone for Duchenne Muscular Dystrophy - Neurology® Journals
Wellstone Muscular Dystrophy Cooperative Research Center - UT Southwestern
Acquisition of Edgewise Therapeutics’ Muscular Dystrophy Business - Servier
Unlocking new paths in muscular dystrophy treatment - University of Nevada, Reno
Interpreting Long-Term MESA Data of Sevasemten to Treat Becker Muscular Dystrophy - NeurologyLive
An Antibody–Oligonucleotide Conjugate for Myotonic Dystrophy Type 1 - The New England Journal of Medicine
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
Muscular Dystrophy Association Announces $100,000 Investment to Advance LGMD Care at Leading MDA Care Centers with BridgeBio - Muscular Dystrophy Association
FDA accepts BridgeBio’s application for potential first limb-girdle muscular dystrophy drug - BioSpace
Breakthroughs in treatment offer hope for rare Duchenne muscular dystrophy - WISH-TV
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
A Decade of Strength: Muscular Dystrophy Association and Burn Boot Camp Team Up for 10th Annual ‘Be Their Muscle’ Campaign - Muscular Dystrophy Association
Biogen to Share New SMA Data at Muscular Dystrophy Association and SMA Europe Conferences - Biogen
Test-Retest Reliability of Remote Assessments in Patients With Myotonic Dystrophy Type 1 - Neurology® Journals
Undiagnosed Maternal Myotonic Dystrophy Type 1 Revealed by Congenital Myotonic Dystrophy in the Neonate - Cureus
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
Researchers provide answers to progressive heart problems in muscular dystrophy and potential reversibility - Baylor College of Medicine Blog Network -
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
Science & Medicine: Why are neurodevelopmental disorders common in Duchenne muscular dystrophy? - Texas Public Radio | TPR
HDAC11 protein identified as potential target for Duchenne muscular dystrophy - Drug Target Review
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
Muscular Dystrophy Association Welcomes Amanda Baze Hall to Board of Directors - Muscular Dystrophy Association
An antibody-siRNA conjugate could treat myotonic dystrophy - BioXconomy
Gene therapy for Bietti crystalline corneoretinal dystrophy: A phase 1/2 clinical trial - ScienceDirect.com
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
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)
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
Givinostat provides durable clinical benefits for patients living with Duchenne Muscular Dystrophy - Drug Discovery News
Muscular Dystrophy Association Announces Łukasz Sznajder, PhD, MSc, to Receive Inaugural MDA Research Momentum Award - Muscular Dystrophy Association
Students Raise 1 Mln in GEL for Children with Duchenne Dystrophy as Parents Fight for Modern Treatments - Civil Georgia
Mouse model reveals unsuspected effects of muscular dystrophy in the GI - Baylor College of Medicine Blog Network -
Give your opinion on a genetically modified medicine against Duchenne Muscular Dystrophy - FPS Public Health
Designer featured on Gardening Australia fears NDIA change a threat to his life - ABC News & Headlines – Australian Broadcasting Corporation
Jet2 colleague raises over £2,000 for Muscular Dystrophy UK - Jet 2.com
Top 10 muscular dystrophy news stories of 2025 - Muscular Dystrophy News
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
Expert Consensus on Genetic Diagnostic Approaches for Patients With Limb-Girdle Muscular Dystrophy - Neurology® Journals
Quantitative 3D assessment of muscle dystrophy through X-ray phase-contrast tomography - Nature
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
Upper limb function and quality of life in Duchenne muscular dystrophy: a cross-sectional study in Chile - Nature
Diversity challenges and reconciles genetics in facioscapulohumeral muscular dystrophy - Nature
Limb-Girdle Muscular Dystrophy: Background, Epidemiology, Etiology - Medscape
UAlbany, VCU to share $6.5M to Launch Muscular Dystrophy Research Center - University at Albany
Limb-Girdle Muscular Dystrophy Scientific Workshop - Neurology® Journals
Muscular Dystrophy Association Announces nearly $2 Million in Collaborative Research Grants Advancing Treatments Across Multiple Neuromuscular Diseases - Muscular Dystrophy Association
Longitudinal Changes of Motor Function in Becker Muscular Dystrophy - Neurology® Journals
Muscular Dystrophy Association Announces More Than $2.7 Million For Research Grants to Advance Breakthroughs Across Neuromuscular Diseases - Muscular Dystrophy Association
Characterizing white matter hyperintensities in myotonic dystrophy type 1 through IVIM derived metrics - Nature
Muscular Dystrophy Association Names Sharon Hesterlee, PhD, as President and Chief Executive Officer - Muscular Dystrophy Association
Muscular Dystrophy Association Honors National Family Caregivers Month with Advocacy and Awareness Nationwide - Muscular Dystrophy Association
Disease Progression and Quality of Life in Duchenne Muscular Dystrophy - NeurologyLive
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)
Living with Muscular Dystrophy - Centers for Disease Control and Prevention | CDC (.gov)
Canadian affiliates recognized by Muscular Dystrophy Canada - IAFF
AAV microdystrophin gene replacement therapy for Duchenne muscular dystrophy: progress and prospects - Nature
CSF Proteomic Profiling Reveals Altered Pathways in Myotonic Dystrophy Type 1 (P2-11.029) - Neurology® Journals
Muscular Dystrophy Research and Tracking - Centers for Disease Control and Prevention | CDC (.gov)
Impaired myogenesis in limb girdle muscular dystrophy type 2B - Nature
Muscular Dystrophy Association & Magic Wheelchair Team Up for Halloween Week Instagram Sweepstakes October 27-29 - Muscular Dystrophy Association
Assessing Delays in Time to Diagnosis of Duchenne Muscular Dystrophy: A Survey of Current Primary Care Practices - Cureus
What Is the Life Expectancy in Duchenne Muscular Dystrophy? - Healthline
Clinician Brief: Muscular Dystrophy - Centers for Disease Control and Prevention | CDC (.gov)
Applications Now Open for MDA’s 2026 Summer Camp Season - Muscular Dystrophy Association
Data Summary: Muscular Dystrophy - Centers for Disease Control and Prevention | CDC (.gov)
Limb-Girdle Muscular Dystrophy Type 2B and Morbihan Disease: A Case Report With an Atypical Presentation - Cureus
CUHK scientists reveal a new mechanism by which myotonic dystrophy type 1 damages the nervous system - CUHK Communications and Public Relations Office
Consensus-based care recommendations for adults with myotonic dystrophy type 2 - Neurology® Journals
Living with Duchenne Muscular Dystrophy: Adrian's Story - Johns Hopkins Medicine
Muscular Dystrophy Association Advocates to Congress on November 4: Every Moment Matters in the Fight Against Muscle Loss - Muscular Dystrophy Association
Isolated Transaminitis as a Sentinel Sign of Duchenne Muscular Dystrophy in an Infant: A Case Report - Cureus
Stem/progenitor cell-based therapy for Duchenne muscular dystrophy - Frontiers
Perioperative Considerations in a Patient With Oculopharyngeal Muscular Dystrophy: A Case Report - Cureus
Skeletal muscle stem cells modulate niche function in Duchenne muscular dystrophy mouse through YY1-CCL5 axis - Nature
SNUPN deficiency causes a recessive muscular dystrophy due to RNA mis-splicing and ECM dysregulation - Nature
Sarepta Therapeutics Announces Pipeline Progress for Multiple Limb-Girdle Muscular Dystrophy Programs - Sarepta Therapeutics
New Discovery Enables Gene Therapy for Muscular Dystrophies, Other Disorders - University of Rochester Medicine
Muscle stem cells in Duchenne muscular dystrophy exhibit molecular impairments and altered cell fate trajectories impacting regenerative capacity | Cell Death & Disease - Nature
Transcriptional adaptation upregulates utrophin in Duchenne muscular dystrophy - Nature
New Gene Therapy for Duchenne Muscular Dystrophy - Johns Hopkins Medicine
Foreign Language Equivalents
Foreign Language Equivalents of 'dystrophy'
Language Equivalent   Language Equivalent
French    Spanish
Misspellings - Typos
ddystrophy,   dtstrophy,   dystropyh,   dystriphy,   dystroohy,   dystorphy,   systrophy,   dytrophy,   dysteophy,   dyystrophy,   dyatrophy,   dysttrophy,   dystrohy,   dysrrophy,   dystropgy,   dystroophy,   ystrophy,   dystrphy,   dystrpohy,   dystroph,   dystrophyy,   dytsrophy,   dysstrophy,   dystropphy,   dydtrophy,   dystrophhy,   dystropht,   dysyrophy,   dystro[hy,   dystrohpy,   dystophy,   dsytrophy,   dystrpphy,   ydstrophy,   dustrophy,   dystrophu,   dysttophy,   dystropy,   fystrophy,   dystrrophy,   dysrophy,   dysrtophy,   dystropjy,   dstrophy
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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