Category - Muscular dystrophies & myopathies

Articles

Are childhood myopathies diagnosed differently?

Are clinical trials for muscular dystrophies and myopathies available in the UK?

Are family members routinely offered genetic counselling and testing in the UK?

Are inflammatory myopathies linked to problems in the immune system?

Are most muscular dystrophies caused by faults in specific genes?

Are muscular dystrophies always inherited, unlike some myopathies?

Are muscular dystrophies and myopathies always progressive conditions?

Are muscular dystrophies and myopathies classed as rare diseases in the UK?

Are muscular dystrophies more common in boys than girls in some types?

Are new gene or exon-skipping therapies available for certain muscular dystrophies?

Are people with myopathies at higher risk of chest infections?

Are regular bone-density checks needed if long-term steroids are used?

Are there disease-modifying treatments for any muscular dystrophies yet?

Are there extra pregnancy checks for women with muscle weakness or myopathy?

Are there UK charities supporting families with muscular dystrophies and myopathies?

Can a new genetic mutation cause a muscular dystrophy with no family history?

Can adults with myopathy or muscular dystrophy work full-time?

Can carriers of muscular dystrophy genes have mild muscle symptoms?

Can certain medicines or statins trigger a toxic myopathy?

Can children with muscular dystrophy attend mainstream school in the UK?

Can children with myopathies take part in PE or adapted sport at school?

Can contractures and scoliosis develop in long-standing muscular dystrophy?

Can environmental factors influence the severity or progression of muscular dystrophies or myopathies?

Can facial or eyelid weakness be part of certain muscular dystrophies?

Can good multidisciplinary care stabilise quality of life with muscular dystrophies and myopathies?

Can inflammatory myopathies go into long-term remission with treatment?

Can inflammatory myopathies go into remission?

Can MRI of muscles help differentiate different myopathies?

Can muscular dystrophies and myopathies affect both children and adults?

Can muscular dystrophies and myopathies be mild and slowly progressive?

Can muscular dystrophies and myopathies shorten life expectancy?

Can muscular dystrophies cause frequent falls or clumsiness at school age?

Can myopathies affect heart and breathing muscles as well as limb muscles?

Can myopathies mimic other muscle disorders?

Can newborn screening detect some muscular dystrophies?

Can occupational therapy help with daily living and equipment needs?

Can people with myopathies safely go through pregnancy and birth?

Can people with these muscle conditions access Personal Independence Payment (PIP) or other benefits?

Can powered wheelchairs or mobility scooters improve independence?

Can pre-implantation genetic testing help avoid passing on muscular dystrophy?

Can respiratory support or cough-assist devices help advanced muscle weakness?

Can steroids help in some myopathies but not in muscular dystrophies?

Can swallowing difficulties be caused by a muscular dystrophy or myopathy?

Can viral infections trigger autoimmune myopathies in adults?

Do muscular dystrophies and myopathies cause calf enlargement or wasting?

Does a myopathy usually cause muscle pain, stiffness or mainly weakness?

Does having another autoimmune disease increase risk of an inflammatory myopathy?

How are breathing problems tracked in progressive myopathies?

How are children with muscular dystrophy followed up in paediatric services?

How are heart complications monitored over time in muscular dystrophy?

How are muscular dystrophies diagnosed by UK specialists?

How can carers and family members best support daily living with muscular dystrophy or myopathy?

How can families get clear information about prognosis and treatment options in the UK system?

How can homes be adapted for progressive muscle weakness?

How can I find out if I’m eligible for a research study or new treatment?

How can my GP refer me to a neuromuscular specialist service?

How can pressure sores and joint problems be prevented in non-ambulant patients?

How common are muscular dystrophies and myopathies in the UK?

How do muscular dystrophies and myopathies affect driving and vehicle adaptations?

How do muscular dystrophies and myopathies affect hobbies, sport and travel?

How does muscle weakness from a myopathy typically present in adults?

How important is physiotherapy in managing muscular dystrophies and myopathies?

How is lung and heart function checked in muscular dystrophy and myopathy?

How long can it take to get a firm diagnosis of a rare myopathy on the NHS?

How often should cardiology and respiratory reviews happen in advanced muscle disease?

How often should treatment plans be reviewed in a neuromuscular clinic?

How should families discuss hereditary muscular dystrophies with children as they grow up?

Is there a family history pattern with common muscular dystrophies?

What are metabolic myopathies?

What are mitochondrial myopathies?

What are mitochondrial myopathies?

What are mitochondrial myopathies?

What are muscular dystrophies and how are they different from myopathies?

What are the first signs of a muscular dystrophy in a child?

What blood tests are used to screen for myopathies and muscular dystrophies?

What community therapy and wheelchair services are available on the NHS?

What does a “myopathy” mean in medical terms?

What does it mean to have a "muscle-wasting" muscular dystrophy?

What emotional and mental health support is available for people with these conditions?

What is dermatomyositis?

What is inclusion body myositis?

What is polymyositis?

What is polymyositis?

What is the role of genetic testing in diagnosing muscular dystrophies?

What key questions should I ask at my next neuromuscular clinic appointment about muscular dystrophies and myopathies?

What medicines are used to treat inflammatory myopathies?

What NHS specialist centres exist for muscular dystrophies and myopathies in the UK?

What reproductive options exist for carriers of muscular dystrophy genes in the UK?

What role do UK patient registries play in muscular dystrophy and myopathy research?

What school adaptations help pupils with muscular dystrophies or myopathies?

What support do families get when a child is diagnosed with a muscular dystrophy?

What workplace adjustments are common for people with these muscle conditions?

When are feeding tubes considered in progressive muscular dystrophy or myopathy?

When do teenagers with muscular dystrophy or myopathy transfer to adult services?

When does shortness of breath suggest muscle weakness in these conditions?

When is a muscle biopsy needed for suspected myopathy?

When should a GP refer to a neuromuscular clinic for muscle weakness?

When should parents ask a GP to check for muscular dystrophy or myopathy?

+ 90 Articles

Show Remaining Articles