Showing posts with label DYSTROPHY. Show all posts
Showing posts with label DYSTROPHY. 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.



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