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Signs and symptoms of Duchenne muscular dystrophy (DMD)
2:59
YouTubePTC Therapeutics
Signs and symptoms of Duchenne muscular dystrophy (DMD)
Dr. Luca Bello discusses the importance of early diagnosis of Duchenne Muscular Dystrophy (DMD) and how to recognise the early signs and symptoms (muscle weakness, not walking by 16-18 months, calf hypertrophy, cognitive and speech delay). If you suspect Duchenne perform a creatine kinase (CK) test. If you are a healthcare professional residing ...
7.2K viewsJan 16, 2020
Duchenne Muscular Dystrophy Symptoms
Duchenne Muscular Dystrophy: Symptoms, Causes, Diagnosis And Treatment
Duchenne Muscular Dystrophy: Symptoms, Causes, Diagnosis And Treatment
onlymyhealth.com
Mar 14, 2024
💡 What does “severe phenotype” mean in Duchenne muscular dystrophy (DMD)? When doctors talk about a phenotype, they’re referring to the way a condition shows up in someone’s body, the physical traits and symptoms that result from their genetics. In Duchenne, a severe phenotype usually means the condition progresses more quickly, often with earlier loss of abilities like walking, climbing stairs, or raising arms. This can also bring earlier complications with breathing, heart health, and other a
0:15
💡 What does “severe phenotype” mean in Duchenne muscular dystrophy (DMD)? When doctors talk about a phenotype, they’re referring to the way a condition shows up in someone’s body, the physical traits and symptoms that result from their genetics. In Duchenne, a severe phenotype usually means the condition progresses more quickly, often with earlier loss of abilities like walking, climbing stairs, or raising arms. This can also bring earlier complications with breathing, heart health, and other a
FacebookHarrison & Duchenne -
1.6K views1 month ago
Duchenne muscular dystrophy (DMD) is a devastating genetic condition that results in progressive muscle weakness, spinal deformities, heart failure and early mortality. While genetic therapies are being explored, current treatments only alleviate symptoms. However, MCW’s Dr. Brian Lin and his lab are researching a promising approach that examines a calcium channel which becomes hyperactive in DMD and how inhibiting that channel could counteract the leading cause of death in DMD patients. Learn m
1:49
Duchenne muscular dystrophy (DMD) is a devastating genetic condition that results in progressive muscle weakness, spinal deformities, heart failure and early mortality. While genetic therapies are being explored, current treatments only alleviate symptoms. However, MCW’s Dr. Brian Lin and his lab are researching a promising approach that examines a calcium channel which becomes hyperactive in DMD and how inhibiting that channel could counteract the leading cause of death in DMD patients. Learn m
FacebookMedical College of Wisconsin
822 views9 months ago
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