Showing posts with label Muscular. Show all posts
Showing posts with label Muscular. Show all posts

Tuesday, 4 April 2017

DELAY IN AGE OF WALKING CAN HERALD MUSCULAR DYSTROPHY IN BOYS WITH COGNITIVE DELAYS


The timing of a toddler's first steps is an important developmental milestone, but a slight delay in walking is typically not a cause of concern by itself.

Now a duo of Johns Hopkins researchers has found that when walking and cognitive delays occur in concert, the combination could comprise the earliest of signals heralding a rare but devastating disorder known as Duchenne muscular dystrophy (DMD).

The study, published ahead of print in The Journal of Pediatrics and conducted by a medical student and a pediatric neurologist, reveals that delays in the onset of walking -- which should occur between 9 and 16 months of age -- are common among boys with DMD and often happen alongside cognitive delays. That combination, the investigators say, can give pediatricians a critical early diagnostic clue and tip them off to the presence of DMD.

"Our review of patient records shows that delayed walking along with cognitive delays represents an ominous combination that should prompt pediatricians to conduct further testing and could speed up diagnosis and treatment," says Kara Mirski, a fourth-year medical student at the Johns Hopkins University School of Medicine. "Earlier diagnosis means that we can start treating these kids sooner and greatly improve their long-term outcomes."

DMD is caused by a defective muscle protein. It is marked by progressive loss of muscle strength and function and, eventually, inability to walk at all. In its advanced forms, the condition can also compromise the function of the heart and breathing muscles. DMD, which almost exclusively affects males, is estimated to occur in one out of 3,500 boys.

Current guidelines from the American Academy of Neurology and the Child Neurology Society do not include DMD on the suspected diagnoses list for boys with developmental delays. While neither cognitive delays nor delayed walking by themselves are necessarily caused by DMD, when the two occur in tandem they should raise the index of suspicion and seriously narrow the range of diagnostic possibilities, the team says.

"The bottom line is that any delay in walking should lead to further probing, or at least vigilant monitoring, and when late walking occurs in the context of other developmental delays, it should put DMD on every pediatrician's radar as a possible cause," says study author Tom Crawford, M.D., a pediatric neurologist and muscular dystrophy expert at the Johns Hopkins Children's Center.
Once a physician suspects DMD, a child can be screened further with a cheap and widely available test that measures the blood levels of creatinine kinase (CK), a protein released as a result of muscle damage or muscle cell death. Normal CK levels rule out DMD.

Once diagnosis is made, treatment with steroids and physical therapy can halt or slow muscle damage and help preserve mobility and function, the researchers say. In addition, because most cases of DMD are inherited, earlier diagnosis would allow families to consult a genetic counselor who can help them make informed decisions about subsequent pregnancies.

DMD can be easily missed during the infant and toddler years, even among children with developmental delays, Crawford notes. The condition's characteristic muscle weakness does not present at such an early age, and the absence of the disease's defining symptom can easily throw off pediatricians. This is why, Crawford says, any developmental delay should prompt pediatricians to probe deeper.
In addition, while most cases of DMD stem from inherited genetic defects, some genetic mutations can arise spontaneously in families without history of the disorder. In those cases, diagnosis can be delayed even further, until a child is 5 or 6 years old, the researchers say.

For the study, the investigators examined the clinical records of 107 children with DMD referred to the Johns Hopkins Children's Center between 1989 and 2012 for diagnosis or treatment. Nearly half (42 percent) had a history of delayed walking (age 16 months or later). Toddlers who started walking late were three times as likely to have cognitive delays as those who began walking on time. The link between the time of a child's first steps and cognitive delay persisted even when investigators eliminated other factors such as the speed and severity of muscle degeneration or age of diagnosis. The study also revealed that DMD patients who started walking late were not referred for diagnostic work-up any earlier than their counterparts who started walking at what is deemed a typical age. In other words, delayed walking did not emerge as the red flag it should have been, the investigators say.



Thursday, 23 March 2017

Neuro Muscular Diseases Vid


Today's video from aboutperipheralneuropathy.blogspot.nl (see link below) talks about neuro-muscular diseases in general, including neuropathy. ALS and muscular dystrophy are perhaps the best known but peripheral neuropathy falls into the same group of disorders. As anybody with neuropathy knows, the effect of nerve damage on muscular activity can be life changing. Many people also worry they have muscular dystrophy, or something else, even if they have been diagnosed with peripheral neuropathy. This video helps to clear up the differences and explains how diagnoses are made using various tests.
The doctor and his practice are from West Michigan but the information he gives applies everywhere.




http://aboutperipheralneuropathy.blogspot.nl/2013/09/how-to-diagnose-peripheral-neuropathy.html

Wednesday, 8 March 2017

Intra Muscular Vitamin D Injections Reduce Neuropathy Symptoms


Today's post from vitamindcouncil.org (see link below) makes some remarkable claims about the benefits of a single, high-dosage injection of vitamin D for neuropathy patients. The results were seen after some weeks and had no effect on the disability of a patient but definitely on the severity of their symptoms. Personally, I find it an encouraging research but it definitely needs some significant follow-up to confirm its conclusions. The injections were intra-muscular and therefore administered by a doctor or medical professional, which may be a good thing, to dissuade people from rushing to the supplement store to swallow 600,000 IU of vitamin D in pill form in one go! Vitamin D supplementation has been a buzz therapy among the neuropathy communities for some time now but most doctors will agree that vitamin D supplementation is only really necessary if there is proven vitamin D deficiency. The word has it that it is certainly beneficial for nerve health but you need to do more of your own research and consult with a trusted medical professional before embarking on a self-help course of vitamin D. Most articles place an emphasis on diabetes-related neuropathy patients but as we all know by now, that's only because the vast majority of neuropathy sufferers come from the diabetic community. Most information regarding neuropathy applies to the condition irrespective of its cause. More articles can be found by using the search button to the right of this blog.

Research finds vitamin D to be a safe and effective treatment for painful diabetic neuropathy
Posted on April 11, 2016 by Amber Tovey

A new study published in the journal BMJ Open Diabetes Research and Care discovered that treatment with a single intramuscular dose of 600,000 IU of vitamin D in patients with painful diabetic neuropathy caused significant reductions in symptoms.

Diabetic neuropathy is a type of nerve disorder that can occur if a person has diabetes. High blood sugar can injure nerves throughout the body, but diabetic neuropathy most commonly affects nerves in the legs and feet. It often causes pain and numbness in the extremities, but may also cause problems in the gastrointestinal tract, urinary tract, blood vessels and heart.

Approximately 21% of the population is affected by painful diabetic neuropathy. Treatments for diabetic neuropathy are limited. The therapeutic effectiveness for all medications is at best near 50% pain relief. In addition, most of the medications are accompanied by unwanted side effects. This has left the medical community searching for new treatments.

A previous study suggested vitamin D supplementation may help treat diabetic neuropathy. The researchers found that weekly vitamin D supplementation of 50,000 IU for 8 weeks reduced symptoms but not disability. In an effort to confirm the treatment effect of vitamin D on diabetic neuropathy, researchers recently conducted a prospective open-labeled trial in Pakistan.

A total of 143 patients with type 1 or type 2 diabetes were included in the study. All patients received a single intramuscular dose of 600,000 IU of vitamin D3.


Pain was assessed using three different questionnaires: The Douleur Neuropathique 4 (DN4), total McGill pain and Short Form McGill Pain Questionnaire (SFMPQ). The researchers wanted to compare pain severity before and after the administration of the vitamin D injection. Here is what they found:
Average vitamin D levels increased from 31.7 ng/ml at baseline to 46.2 ng/ml at week 20.
Total McGill pain score, DN4 and SFMPQ significantly decreased after vitamin D administration (p is less than 0.001).

The researchers concluded,

“The administration of 600 000 IU of vitamin D results in a modest but significant increase in 25(OH)D levels measured at 20 weeks. This improvement in 25(OH)D levels was associated with an improvement in several independent measures of PDN, which became significant approximately 10 weeks after administration of vitamin D.”

The researchers noted that the average vitamin D levels of the patients at baseline was much higher than previous studies, indicating that a proportion had likely received vitamin D supplementation from their primary physician previously. This shows vitamin D supplementation has become a more widely accepted practice for diabetic patients.

Future studies should follow a randomized controlled trial design and use a daily dosage regimen.

Citation

Tovey, A.; Cannell, JJ. Research finds vitamin D to be a safe and effective treatment for painful diabetic neuropathy. The Vitamin D Council Blog ; Newsletter, 2016.

https://www.vitamindcouncil.org/blog/research-finds-vitamin-d-to-be-a-safe-and-effective-treatment-for-painful-diabetic-neuropathy/

Saturday, 19 November 2016

HOMOEOPATHIC REMEDIES FOR MUSCULAR DYSTROPHY


Muscular dystrophy is a group of diseases that cause progressive weakness and loss of muscle mass. In muscular dystrophy, abnormal genes (mutations) interfere with the production of proteins needed to form healthy muscle.
There are many different kinds of muscular dystrophy. Symptoms of the most common variety begin in childhood, primarily in boys. Other types don't surface until adulthood.
Some people who have muscular dystrophy will eventually lose the ability to walk. Some may have trouble breathing or swallowing
Causes-Certain genes are involved in making proteins that protect muscle fibers from damage. Muscular dystrophy occurs when one of these genes is defective.
Each form of muscular dystrophy is caused by a genetic mutation particular to that type of the disease. Many of these mutations are inherited. But some occur spontaneously in the mother's egg or the developing embryo and can be passed on to the next generation
Symptoms- The main sign of muscular dystrophy is progressive muscle weakness. Specific signs and symptoms begin at different ages and in different muscle groups, depending on the type of muscular dystrophy
The day to day activities of the patient is affected. Some of them are-inability to walk, poor balance, loss of bowel control, drooping eyelids, waddling gait, respiratory difficulty, limited range of movements, frequent falls, loss of strength in a muscle or a group of muscles as an adult, low muscle tone (hypotonia), joint contracture (club foot, claw hand or others), abnormally curved spine (scoliosis)
Some types involve heart muscles, causing cardiomyopathy or disturbed heart rhythm (arrhythmias)
HOMOEOPATHIC REMEDIES

Homeopathic treatment helps to slow down the process of muscular degeneration, and can work on bringing some symptomatic relief, such as improving muscle power. It is aimed at better quality life.
Homeopathic medicines are prescribed after the detailed case study consisting of physical, emotional and genetic make up of an individual. Homeopathic medicines help to reduce the muscle weakness and control the disease progression. There are some specific Homeopathic remedies, which help for muscle paralysis and weakness and which have been found effective in the treatment of Muscular Dystrophy. Homeopathic treatment is recommended.
PLUMBUM METALLICUM 1000-- It is the head remedy and covers symptoms from simple irritation to complete destruction of muscles.Complete loss of sensation, weakness, cutting, gripping, trembling, twisting , shooting in the neck, contraction  and atrophy of the deltoid, edema, unsteady gait, shortening of muscles. Worse at night and from motion
ARGENTUM NIT. 30- Sensitiveness of spine, great pain in spine which is worse at night. Great trembling and weakness of extremities , cannot walk with eyes closed, rigidity of calves, also debility. Walks and stands unsteadily. Worse at night and from cold, better from fresh air
PHOSPHORUS 30- It has hypertrophy in some parts and atrophy in others. The patient is tall, hollow chested, with tubercular or syphilitic diathesis. Burning and trembling , numbness and weakness are the main symptoms
THALLIUM 200- Muscular atrophy . Pain in locomotar ataxia. Tremors. Pain in stomach and bowels like electric shocks
KALI PHOS 30-For muscular atrophy.It should be given along with other remedies
ARNICA MON. 30, CUPRUM MET. 30, BARYTA IOD. 30- They may be tried in the given order when the above remedies fail














Tuesday, 19 July 2016

HOMOEOPATHIC REMEDIES FOR MUSCULAR ATROPHY


Muscle atrophy is the wasting or loss of muscle tissue.There are two types of muscle atrophy.
·         Disuse atrophy occurs from a lack of physical activity. In most people, muscle atrophy is caused by not using the muscles enough. People with seated jobs, medical conditions that limit their movement, or decreased activity levels can lose muscle tone and develop atrophy. This type of atrophy can be reversed with exercise and better nutrition. Bedridden people can have significant muscle wasting. Astronauts who are away from the Earth's gravity can develop decreased muscle tone after just a few days of weightlessness.
·         The most severe type of muscle atrophy is neurogenic atrophy. It occurs when there is an injury to, or disease of, a nerve that connects to the muscle. This type of muscle atrophy tends to occur more suddenly than disuse atrophy.
Cause-Some muscle atrophy occurs normally with aging. Other causes may include:Alcohol-associated myopathy, Amyotrophic lateral sclerosis (ALS or Lou Gehrig's disease), Burns, Burns, Guillain-BarrĂ© syndrome, Injury, Long-term corticosteroid therapy, Malnutrition , Motor neuropathy, Muscualr dystrophy and other diseases of the muscle, Not moving (immobilization), Osteoarthritis , Polio, Rheumatoid arthritis, Spinal cord injury, Stroke
HOMOEOPATHIC REMEDIES
PLUMBUM METALLICUM  200—CM--A specific remedy . It covers symptoms from simple irritation to complete destruction of muscles. It not only covers the muscles of brain but also of the trunk, extremities and muscles of other organs. Complete loss of sensation, weakness, cutting, gripping, trembling, twisting, shotting in the neck, contraction and atrophy of deltoid , oedema, unsteady gait, shortening of muscles. Worse at night and from motion
BARYTA CARB. 200-- Muscular atrophy at the age of puberty          
PHOSPHORUS 200- It has hypertrophy in some parts and atrophy in others.Tall patient, hollow chested individual with tubercular or syphilitic diathesis. Burning with trembling, numbness and weakness are the ranking symptoms
MURIATIC ACID 30—It cures muscular weakness following the excessive use of
opium
THALLIUM 200- Muscular atrophy. Pain in  locomotar ataxia. Tremors. Pain in stomach and bowels like electric shocks
KALI PHOS 200- It is a constitutional remedy and should be given along with other remedies
ARNICA MONTANA 30 , CUPRUM METALLICUM 30- , BARYTA IODIDE 30—Alternate these remedies when well indicated remedies fail
ARNICA MONTANA 30 and RHUS TOXICODENDRON 30—Alternate these remedies , it acts as a muscular tonic
CAUSTICUM 200- CM—Paralysis of single parts. Heaviness and weakness . Restless leg at night. Unsteady walking and easily falling
MEDORRHINUM 10 M—Prevent recurrence