Genetic heart

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Becker muscular dystrophy is an inherited disorder that involves slowly worsening muscle weakness of the legs and pelvis. Symptoms:- Muscle weakness, slowly progressive (Difficulty running, hopping, jumping; Progressive difficulty walking) Toe-walking (walking on toes) Use of Gower's Maneuver or a modified form of Gower's Maneuver to get up from floor. Ability to walk may continue well into adulthood. (Very variable.) Frequent falls Difficulty breathing Non progressive cognitive dysfunction only in rare cases: not as common as in Duchenne Muscular Dystrophy because the brain only needs small amounts of dystrophin. Skeletal deformities, chest and back (scoliosis) Muscle deformities (contractions of heels, legs; Pseudohypertrophy of calf muscles) Fatigue Heart disease Elevated CPK (creatine phosphokinase) levels in blood: Elevated CK levels are more common at younger ages and decreases later in life, perhaps due to the fact that muscle degeneration occurs more rapidly at younger ages, when there is also more muscle mass to deteriorate. Tests:- Creatine kinase (CPK) levels may be elevated. An electromyography (EMG) shows that weakness is caused by destruction of muscle tissue rather than by damage to nerves. Genetic testing A muscle biopsy (immunohistochemistry or immunoblotting) or Genetic test (blood test) confirms the diagnosis. Treatment:- There is no known cure for BMD, although homoeopathic medicine is showing promising vectors that may replace damaged muscle tissue. Treatment is generally aimed at controlling the onset of symptoms to maximize the quality of life, prevent further detoriation leading to gradual improvement in health status of patients. We have more than patients of all types of muscular dystrophy from all over the world. We have documented up to 80% improvement in our patients. Recently Dr. Ramesh Bhardwaj has been awarded with "THE MOST SUCCESSFUL PHYSICIAN FOR TREATING MUSCULAR DYSTROPHY" For details contact:- Dr. Ramesh Bhardwaj homoeopathic world, Noida, India

Muscular dystrophy refers to a group of genetic, hereditary muscle diseases that cause progressive muscle weakness. Muscular dystrophy are characterized by progressive skeletal muscle weakness, defects in muscle proteins, and the death of muscle cells and tissue. Nine diseases including Duchenne, Becker, limb girdle, congenital, facio scapulohumeral, myotonic, oculopharyngeal, distal, and Emery-Dreifuss are always classified as muscular dystrophy. Duchenne muscular dystrophy (DMD) is the most common childhood form of muscular dystrophy. DMD usually becomes clinically evident when a child begins walking. Patients typically require a wheelchair by age 10 to 12 and die in their late teens or early 20s. In the early s, researchers identified the gene for the protein dystrophin which, when absent, causes DMD. The dystrophin gene is the largest known gene in humans. Since the gene is on the X-chromosome, this disorder affects primarily males. Females who are carriers have milder symptoms. Sporadic mutations in this gene occur frequently, accounting for a third of cases. The remaining two-thirds of cases are inherited in a recessive pattern. age at onset: two to six years; symptoms include general muscle weakness and wasting; affects pelvis, upper arms, and upper legs; eventually involves all voluntary muscles; survival beyond 20 years is rare. Dystrophin is part of a complex structure involving several other protein components. The "dystrophin-glycoprotein complex" helps anchor the structural skeleton within the muscle cells, through the outer membrane of each cell, to the tissue framework that surrounds each cell. Due to defects in this assembly, contraction of the muscle leads to disruption of the outer membrane of the muscle cells and eventual weakening and wasting of the muscle. symptoms * Progressive Muscular weakness * Poor Balance * Frequent Falls * Walking Difficulty * Waddling Gait * Calf Pain * Limited Range of Movement * Muscle Contractual * Respiratory Difficulty * Drooping Eyelids * Scoliosis (curvature of the spine) * Inability to walk Some types of Muscular Dystrophy can affect the heart, causing cardiomyopathy or arrhythmias. The prognosis for people with muscular dystrophy varies according to the type and progression of the disorder. Some cases may be mild and progress very slowly over a normal lifespan, while others produce severe muscle weakness, functional disability, and loss of the ability to walk. There is no known cure for muscular dystrophy. Inactivity (such as bed-rest and even sitting for long periods) can worsen the disease. Physical therapy, Occupational therapy, speech therapy and orthopedic instruments (e.g., wheelchairs, standing frames) may be helpful. IS THERE A WAY OUT? To a family with a child with muscular dystrophy, it must seem like the worst disease. To what extent might the remedy enable the sufferer to overcome the existing condition? There is considerable good news. Dr. Ramesh Bhardwaj, a senior homeopathic consultant, president of homeopathic medical association has proved that there is a way to lead a healthy and normal productive life for muscular dystrophy. Good diet and homeopathic remedy found to be very effective and successful in muscular dystrophy patients. It is found that, with the start of medicine there is gradual improvement in the patientโ€™s condition with marked improvement in muscle strength, improved sleeping and eating patterns and weight gain within 1-2 months. Early initiation of treatment in the course of this disease can help a lot in reducing future disability and prolonging survival. Patients unable to lift their heads before treatment were able to do so after treatment and their speech and walking ability improved as well. And with long term medicine patient can lead to normal healthy and productive life. "HOMOEOPATHIC TREATMENT IS STRONGLY RECOMMENDED" DR. BHARDWAJ HAS BEEN AWARDED WITH "BEST HOMOEOPATHY FOR TREATING MUSCULAR DYSTROPHY " visit us--www.homoeopathic-world

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