This term refers to a particular rare type of genetic muscle disease that presents with muscle weakness which typically becomes apparent in infancy or early childhood (congenital) and can worsen […]
Read MoreWhat is the role of creatine kinase (CK) determination in the evaluation of muscular dystrophy?
Creatine kinase (CK) is an important protein in muscle cells. It is also found in the heart, brain, and other tissues, but at lower levels. Increased amounts of CK are […]
Read MoreCan the number of deletions on gene 4q be used as an indicator for prognosis for facioscapulohumeral muscular dystrophy ?
Facioscapulohumeral muscular dystrophy (FSHD) typically presents with slowly progressive weakness of the facial muscles, scapular winging and foot drop. The severity is highly variable within and between families. The diagnosis […]
Read MoreDuchenne and Becker muscular dystrophies have similar signs and symptoms. Is there a genetic difference to inform a diagnosis?
Duchenne and Becker muscular dystrophy are part of a spectrum of disease now more correctly called dystrophinopathies, as they are due to genetic faults (mutations) in a gene called dystrophin. […]
Read MoreUse of creatine and steroids
The use of creatine and steroids is dealt with here in response to two questions received. I have muscular dystrophy. Friends have suggested using the supplement creatine to build muscles. […]
Read MoreGenetic testing
What is genetic testing? Genetic testing is a type of medical test that identifies the changes in our genes that cause disease. It is usually performed by studying DNA – […]
Read MoreCare management protocols in South Africa for patients with muscular dystrophies
Care management protocols are a team-based, patient-centred approach designed to assist patients and their support systems in managing medical conditions more effectively. No specific protocols that are nationally approved and […]
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Living a simple life
By Dr Sandra Bredell What does it mean to “live a simple life”? The Merriam-Webster Dictionary describes it as “a manner of living in which a person does not own […]
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Scoliosis in Children with Muscular Dystrophy
By Jason E. Lowenstein, MD. Scoliosis & Spinal Deformity Surgeon Muscular dystrophy (MD) is a genetic disorder that results in progressive muscle wasting. Nine forms of MD exist, each affecting […]
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Breathing problems
By Marisa Wexler In Muscular Dystrophy News Today Last updated Jan. 13, 2022 Muscular dystrophy is a group of conditions characterized by progressive muscle weakness. In addition to affecting muscles […]
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