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Inheritance of Duchenne Muscular Dystrophy (DMD) | Genetics Explained by Dr. Ravinder Dimri

Inheritance of Duchenne Muscular Dystrophy (DMD) | Genetics Explained by Dr. Ravinder Dimri

1.3K views8 months ago

YouTubeConceptual Orthopedics

Genetic testing is part of the Duchenne journey. When a child is diagnosed with Duchenne Muscular Dystrophy, one of the first conversations is usually about genetic counselling and carrier testing. What many people don’t realise is this: 👉 Around 30% of boys born with Duchenne have a spontaneous (new) genetic mutation. That means there is no family history, no warning signs, and nothing anyone did wrong. Duchenne is caused by a change in the gene that makes dystrophin, a protein muscles need to

Genetic testing is part of the Duchenne journey. When a child is diagnosed with Duchenne Muscular Dystrophy, one of the first conversations is usually about genetic counselling and carrier testing. What many people don’t realise is this: 👉 Around 30% of boys born with Duchenne have a spontaneous (new) genetic mutation. That means there is no family history, no warning signs, and nothing anyone did wrong. Duchenne is caused by a change in the gene that makes dystrophin, a protein muscles need to

2.2K views8 months ago

FacebookHarrison & Duchenne - Raising Awareness of Duchenne Muscular Dy…

Duchenne muscular dystrophy (DMD) :Symptoms and management : Gower’s Sign #duchennemusculardystrophy

Duchenne muscular dystrophy (DMD) :Symptoms and management : Gower’s Sign #duchennemusculardystrophy

2.4K views9 months ago

YouTubeDr. Sorabh Gupta Neurologist: Simplified Neurology

Duchenne Muscular Dystrophy | History Taking Explained | Dr. Ravinder Dimri

Duchenne Muscular Dystrophy | History Taking Explained | Dr. Ravinder Dimri

1.5K views8 months ago

YouTubeConceptual Orthopedics

$DEXA scans play an important role in caring for people living with Duchenne muscular dystrophy. A DEXA (dual-energy X-ray absorptiometry) scan is a simple, non-invasive test that measures bone mineral density, usually in the arm or leg. In Duchenne, bones can become thinner and weaker over time, especially with long-term steroid use and reduced mobility. Weaker bones are more likely to fracture, sometimes from minor falls or even everyday movements. Tracking bone density helps the care team unde$

DEXA scans play an important role in caring for people living with Duchenne muscular dystrophy. A DEXA (dual-energy X-ray absorptiometry) scan is a simple, non-invasive test that measures bone mineral density, usually in the arm or leg. In Duchenne, bones can become thinner and weaker over time, especially with long-term steroid use and reduced mobility. Weaker bones are more likely to fracture, sometimes from minor falls or even everyday movements. Tracking bone density helps the care team unde

2K views9 months ago

FacebookHarrison & Duchenne - Raising Awareness of Duchenne Muscular Dy…

Duchenne Muscular Dystrophy: Our Son’s Journey & Diagnosis

Duchenne Muscular Dystrophy: Our Son’s Journey & Diagnosis

563 views6 months ago

YouTubeGardner's Mattress & More

Riley’s Uncertain Duchenne or Becker Diagnosis: Why His Family Pushed for Genetic Testing

Riley’s Uncertain Duchenne or Becker Diagnosis: Why His Family Pushed for Genetic Testing

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Duchenne Muscular Dystrophy (DMD) Awareness and the importance of early diagnosis.

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Duchenne Muscular Dystrophy: Comprehensive Management and Rehabilitative Strategies

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Mental health and Duchenne muscular dystrophy

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YouTubeGENEration Hope

Gower Sign Explained | Duchenne Muscular Dystrophy | Dr. Ravinder Dimri

2.3K views8 months ago

YouTubeConceptual Orthopedics

DIAGNOSING DUCHENNE 💉🧬 When there’s a concern that a child might have Duchenne Muscular Dystrophy, the first step is usually a simple blood test to check CK (creatine kinase) levels. 📊 Children with Duchenne often have CK levels 10 to 100 times higher than normal, a strong indicator that something’s not right with muscle health. If CK is elevated, doctors will recommend genetic testing to find the exact DNA change (genetic mutation) that causes Duchenne. 🧠 A genetic counsellor can help inter

4.5K views10 months ago

FacebookHarrison & Duchenne - Raising Awareness of Duchenne Muscular Dy…

The Power of Genetic Testing in Duchenne Muscular Dystrophy

608 viewsAug 12, 2024

YouTubeMapmyGenome

DMD Gene Discovery Dystrophin Protein Breakthrough Explained #dystrophin

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Mother welcomes rare drug recommendations but urges wider access | #RTENews

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Current Treatment Strategy in Duchenne Muscular Dystrophy | Dr. Ravinder Dimri

791 views8 months ago

YouTubeConceptual Orthopedics

Gene replacement therapy for Duchenne Muscular Dystrophy (DMD): New documentary from UC Davis Health

32.5K viewsDec 20, 2024

YouTubeUC Davis Health

Harrison’s Life with Duchenne Muscular Dystrophy on Instagram: "Genetic testing is part of the Duchenne journey. When a child is diagnosed with Duchenne Muscular Dystrophy, one of the first conversations is usually about genetic counselling and carrier testing. What many people don’t realise is this: 👉 Around 30% of boys born with Duchenne have a spontaneous (new) genetic mutation. That means there is no family history, no warning signs, and nothing anyone did wrong. Duchenne is caused by a cha

6.7K views8 months ago

Instagramharrison_and_duchenne

Duchenne Muscular Dystrophy Explained in 40 Seconds #DMD #medicalshorts #paediatrics

9.2K views11 months ago

YouTubePW MedEd NEET PG | FMGE | INICET

Gait & Deformities in Duchenne Muscular Dystrophy | Dr. Ravinder Dimri

966 views8 months ago

YouTubeConceptual Orthopedics

Children with Duchenne muscular dystrophy

265 views5 months ago

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Gait Changes in Duchenne Muscular Dystrophy | Gluteus Medius vs Maximus | Dr. Ravinder Dimri

1.4K views8 months ago

YouTubeConceptual Orthopedics

Becker Muscular Dystrophy (BMD)

20 views6 months ago

YouTubeMedicine and Well-being

Duchenne Muscular Dystrophy: A Day in Our Lives

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Life with Profound Autism and Duchenne Muscular Dystrophy

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132.9K views8 months ago

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One of our many trips to the ER. RC wasn’t able to keep anything down, and I couldn’t get his fever to break. When your child has Duchenne Muscular Dystrophy, you don’t take chances. Vomiting and fevers can be serious because long-term steroid use can put him at risk for adrenal insufficiency. Dad was completely wiped out once RC started feeling better. 😂 Meanwhile, RC bounced right back, bright-eyed and bushy-tailed. And me? I stayed in full mom mode the entire time, watching every symptom, ev

33.9K views3 months ago

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