Treat your congenital muscular dystrophy with advanced stem cell treatment in India
Put an end to the agony caused by Congenital Muscular Dystrophy!
Congenital Muscular Dystrophy (CMD) is a serious, life-altering condition affecting muscle development, strength, and mobility. It is a group of genetic neuromuscular disorders that can lead to permanent muscle weakness and disability.
Advances in medical science have enabled doctors to develop innovative treatments and therapies that can alleviate the symptoms of CMD.
Therapies like stem cell transplantation, physical therapy, and pharmacological treatment are helping people with CMD achieve a better quality of life.
In this article, we will look at the different types of CMD, their diagnoses and treatments, and explore the latest advancements in managing this condition.
To start off with here is the story of our hero:
Natalie was a bright and energetic little girl living with her parents, Thomas and Harry. She loved to play outdoors and had a passion for dancing. Unfortunately, when Natalie turned eight, her parents started to notice that she wasn’t keeping up with the other children in activities like running and jumping rope.
At first, her parents thought that it was due to her age, but as time passed they noticed that Natalie’s muscle weakness wasn’t improving. After consulting with several doctors, Thomas and Harry were unable to find a diagnosis for their daughter’s condition.
Desperate for answers, Thomas and Harry searched the internet for more information about their daughter’s condition. After much research, they stumbled upon MedicoExperts.
They quickly contacted MedicoExperts and after examining Natalie, the doctors concluded that she had been diagnosed with Congenital Muscular Dystrophy (CMD). The team at MedicoExperts immediately began implementing a plan of action to help Natalie. They prescribed her therapies and other treatments that helped reduce the symptoms of CMD.
With the help of stem cell therapy, physical therapy, and pharmacological treatment, her muscle strength began to improve. Along with this they also monitored her progress regularly, ensuring that Natalie and her parents had 24/7 access to medical care.
Over the course of a few months, Natalie’s condition began to improve significantly. Her muscles became stronger, her mobility increased and her quality of life was enhanced. With the help of MedicoExperts, Thomas, and Harry were able to provide their daughter with the help and care that she needed.
Natalie’s story is a testament to the power of modern medicine. With the help of a MedicoExperts and cutting-edge treatments, Natalie was able to overcome her Congenital Muscular Dystrophy and live a full and healthy life.
How far we’ve come in understanding and treating this condition. Read on to find out more!
What is congenital muscular dystrophy?
CMD is a type of muscular dystrophy that is noticeable either at or soon after birth. Muscular dystrophies are genetic conditions that mainly affect voluntary muscles and cause them to degenerate over time.
The appearance of muscle abnormalities seen in dystrophic conditions can vary greatly depending on the stage and severity of the disorder.
What causes congenital muscular dystrophy?
Genetic mutations can cause CMD which affects the proteins required for muscles and possibly the eyes and brain.
The extracellular matrix (ECM) is a web-like structure that contains muscle cells. It is made up of various types of proteins that are linked to carbohydrates (known as glycoproteins).
Glycoproteins play various roles in the ECM, such as transferring the force of muscle contraction to the skeleton, linking muscle cells with one another, transmitting signals between cells, and supporting development and repair. The mutation that leads to the loss of glycoproteins affects normal muscle function.
Although it is unclear why CMDs result in earlier muscle weakness compared to other forms of muscular dystrophy. But is possible that the muscle proteins affected in CMD are necessary for the early development of an infant’s muscles, whereas muscle proteins associated with other types of muscular dystrophies become important only when the muscles are used extensively as the child grows.
It is important to understand that the early onset of muscle weakness in CMD does not necessarily mean that the condition is more severe than other types of muscular dystrophy. The extent and speed of muscle weakness progression differ among various forms of CMD and from child to child.
What are the symptoms of congenital muscular dystrophy?
Infants with hypotonia, or low muscle tone, may appear floppy and have difficulty meeting motor milestones like rolling over, sitting up, or walking. This weakness can persist later in life.
CMD, which is characterized by muscle weakness, can cause joint stiffness or looseness.
This condition may lead to:
- Spinal curvature,
- Respiratory insufficiency,
- Intellectual disabilities,
- Learning disabilities,
- Eye defects, or
- Seizures, all this depending on the type of CMD.
How is congenital muscular dystrophy diagnosed?
When diagnosing any type of muscular dystrophy, the doctor typically starts by asking about the patient’s and family’s medical history and conducting a physical exam. By analyzing the weakness pattern, much can be learned from these initial assessments, which can often make the diagnosis without needing complex diagnostic tests.
The doctor needs to determine if the weakness in the patient is due to a muscle problem or a nerve problem that affects the muscles.
A physical examination can typically identify the source of weakness. Nerve conduction studies and electromyography are occasionally conducted as well.
- These tests involve using electricity and extremely small pins to stimulate and evaluate the nerves. Electromyography is typically not very painful, although it can cause discomfort.
- During the initial stage of diagnosis, doctors commonly request a unique type of blood test known as a CK level test. CK refers to creatine kinase, which is an enzyme that exits from injured muscles.
- A doctor may order a muscle biopsy, which involves surgically removing a small sample of muscle from the patient, to determine the disorder that is causing the CK elevation.
- Genetic tests can examine a person’s genes for defects that cause CMD and predict the disease’s potential progression. These tests usually require a blood sample and can also assist families in determining the likelihood of passing on the disease to future generations.
Conventional Treatment for Congenital Muscular Dystrophy
Prior to the introduction of effective treatments for CMD, physical therapy and occupational therapy were the standard of care. These therapies aim to improve body function, reduce pain and discomfort, maintain mobility, and increase independence.
1. Physical Therapy
Physical therapists can help with stretching exercises that treat muscle tightness and promote better posture. They also provide orthotics or braces to support weakened muscles and protect them from injury.
2. Occupational Therapy
Occupational therapists can help the patient learn to do daily activities that are important to their quality of life, such as self-care, communication, and leisure activities. They can also assist with using assistive devices, such as wheelchairs or special equipment like walkers.
3. Medication
Additionally, the doctor may prescribe medications such as muscle relaxants or pain relievers to help reduce muscle spasms and manage chronic pain.
4. Surgery
In some cases, surgical intervention might be needed to repair weakened muscles or correct spinal curvatures.
Advanced Stemcell Treatment for Congenital Muscular Dystrophy
Researchers have proven that stem cell therapy can be used to treat a variety of muscle diseases, including Congenital Muscular Dystrophy (CMD). Stem cell therapy has been shown to have the potential to restore strength and improve physical functioning by repairing damaged muscles. It also helps reduce inflammation, which is a major contributor to CMD-related disability.
The stem cells used in CMD therapy are typically taken from the patient’s fat, bone marrow, or umbilical cord. They can also be sourced from donated umbilical cords and placentas. The stem cells are isolated, purified, and activated before they are injected into the affected muscles. This procedure is done under general anesthesia and typically takes two hours to complete.
This treatment stimulates the repair of damaged tissue and enhances the growth of new healthy cells. This process can potentially reverse some of the symptoms of CMD such as weakened muscles, skeletal abnormalities, and even paralysis.
The results of stem cell therapy for CMD vary from person to person, depending on the severity of the condition. In, patients report significant improvements in strength and function after treatment. Patients may experience reduced pain, improved mobility, and increased independence as a result of the therapy. It’s a safe and effective treatment with minimal side effects.
Stem cell therapy may also be combined with other treatments, such as physical and occupational therapy, to maximize its potential benefits. With the help of advanced stem cell treatments, those living with CMD may be able to achieve a better quality of life.
The Prognosis for Congenital Muscular Dystrophy
The key to successful treatment for CMD is early diagnosis and intervention, so it’s important to talk to your doctor as soon as you experience any of the symptoms associated with CMD.
Stem cell treatment can cure congenital muscular dystrophy. This therapy’s regenerative property provides new hope to individuals suffering from this condition by effectively treating and curing their symptoms.
It is important to diagnose congenital muscular dystrophy early in order to manage it properly. It is also important to understand that there is a good chance for improvement in muscle strength and to prevent joint contractures, which can help the child reach their full potential for walking. Greater awareness is needed regarding these factors.
What is the Cost of stem cell therapy for congenital muscular dystrophy in India?
India is an attractive destination for stem cell therapy due to its world-class hospitals, qualified experts, and affordable treatment costs. Patients can trust the quality of care they receive and benefit from affordability. The stem cell therapy for congenital muscular dystrophy treatment in India is tailored to meet individual patient needs and medical conditions.
Additionally, the cost of stem cell therapy in India is considerably lower than that of other countries, making it an attractive option for those seeking affordable and effective medical care.
The starting price for stem cell therapy for congenital muscular dystrophy treatment in India is USD 2000 per cycle, which may vary depending on the patient’s present condition.
Conclusion
Congenital muscular dystrophy is a debilitating condition that can cause physical and mental impairments. A diagnosis of congenital muscular dystrophy can be distressing, particularly due to its potential impact on a person’s life. But with proper treatments and stem cells, occupational and physical therapies can provide hope by reversing some of the symptoms of CMD.
Consult with MedicoExperts for efficient diagnosis and treatment. The team is well-equipped to provide personalized advice and guidance. Contact the team today and benefit from MedicoExpert’s world-class facilities, experienced experts, and affordable stem cell therapy for congenital muscular dystrophy.
Frequently Asked Questions and patient concerns:
Q1. Can you live a normal life with Congenital muscular dystrophy?
Ans: Yes, with the right treatment and therapies, many people with CMD can live a normal life. The amount of improvement is different for each individual and depends upon the severity of their condition. Although Stem cell therapy has been found to be an effective treatment for CMD, many patients report improved strength, mobility, and independence after undergoing the treatment.
Q2. Which type of congenital muscular dystrophy is the most frequently occurring?
Ans: When infants experience weakness, possible causes could be congenital myopathies such as central core, nemaline road, and centronuclear myopathy. These are the most common differential diagnoses.
Q3. What are the three most common types of muscular dystrophy?
Ans: Muscular dystrophy is a group of disorders that can cause muscle weakness and are typically hereditary. The three most frequently encountered types are Duchenne and Becker muscular dystrophy, myotonic muscular dystrophy, and facioscapulohumeral muscular dystrophy.
Read more about muscular dystrophy here.
Q4. Does congenital muscular dystrophy worsen over time?
Ans: CMD is a condition that typically starts around the time of birth and progresses differently depending on the type. While some types progress slowly, others can shorten a person’s lifespan.
Q5. What are the 4 types of stem cell therapy?
Ans: The four types of stem cell therapy include embryonic stem cell therapy, fetal stem cell therapy, adult stem cell therapy, and induced pluripotent stem cell therapy.
These therapies are used to treat a variety of conditions, including congenital muscular dystrophy. MedicoExperts can help you with the right therapy as per your individual requirements. Contact the team today to learn more about CMD.
Q6. What is the current status of stem cell therapy for the regulatory framework?
Ans: The stem cell-based therapy is in the research phase and not yet formally approved by ICMR. However, the application of stem cells, popularly known as bone marrow transplants, in blood-related disorders is approved by ICMR.
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