Know How Much Angelman Syndrome Treatment Cost In India

Soumya Mishra

, Treatments

Remember moments when a minor inconvenience or disease made you uncomfortable. People who suffer from Angelman Syndrome face much more than that. A child or an adult, or any survivor who suffers from this disease is not able to speak properly, has walking issues, and many other minor disabilities.




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This syndrome has no proper treatment but doctors can help you manage your child’s health to save them from further issues. To know more about Angelman syndrome treatment cost and treatment process you can contact us.  




Know About Angelman Syndrome Treatment Cost




Angelman Syndrome Treatment Cost in India is one-third less than India in comparison to other countries without compromising the treatment quality and support. GoMedii can help you get the best treatment on a budget. 



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What is Angelman Syndrome?




Angelman syndrome is a genetic condition that affects the nervous system and causes severe physical and learning disabilities. People with Angelman syndrome have a near-normal life expectancy, but they need support throughout their life.


Angelman syndrome is a genetic disorder. It causes delayed development, intellectual disability, problems with speech and balance, and, sometimes, seizures.


People with Angelman syndrome generally smile and laugh frequently, and have happy, excitable personalities.


Developmental delays, which begin between 6 and 12 months of age, are usually the first signs of Angelman syndrome. Seizures might begin between the ages of 2 and 3 years old.





What are the symptoms of Angelman Syndrome?




The signs and symbols are noticeable since starting, and the treatment works best if done at the earliest. Visit a doctor if you notice any of these symptoms in your child and get the best treatment. signs and symptoms include:




  • Intellectual disability
  • Developmental delays
  • Not able to speak properly
  • Frequent smiling and laughter
  • Happy, excitable personality
  • Sucking or feeding difficulty
  • Difficulty moving, walking, or balancing well
  • Trouble going to sleep and staying asleep




What causes Angelman Syndrome?




Angelman syndrome is a genetic disorder. It’s usually caused by problems with a gene located on chromosome 15 known as the ubiquitin protein ligase E3A (UBE3A) gene. The causes are: 




  • A missing or defective gene


  • Everyone receives their own pairs of genes from their parents, one copy from their mother and the other from their father.


  • These chromosomes typically use information from both copies, but only one copy is active in a small number of genes.


  • Generally, only the maternal copy of the UBE3A gene is active in the brain. Most cases of Angelman syndrome are caused when part of the maternal copy is missing or damaged.


  • In a few cases, Angelman syndrome occurs when two paternal copies of the gene are inherited, instead of one from each parent.



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What is the diagnosis of Angelman Syndrome?




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The doctor might suspects Angelman syndrome if the child has issues like specifically minimal or difficulty in speaking, and other signs and symptoms of the disorder, such as seizures, problems with movement and balance, a small head size, and a happy demeanor.


A definitive diagnosis can almost always be made through a blood test. This genetic testing can identify abnormalities in the child’s chromosomes that indicate Angelman syndrome.



A combination of genetic tests can reveal the chromosome defects related to Angelman syndrome. These tests might review


Parental DNA patterns. This test is also known as a DNA methylation test, screens for three of the four known genetic abnormalities that cause Angelman syndrome.


Missing chromosomes. A chromosomal microarray (CMA) can show if portions of chromosomes are missing.



Gene mutation. Rarely, Angelman syndrome might occur when a person’s maternal copy of the UBE3A gene is active but mutated. If a DNA methylation test results are normal, the child’s doctor might order a UBE3A gene sequencing test to look for a maternal mutation.



If your child is diagnosed with this syndrome do not take the chance to contact a doctor and get proper treatment. 





How is Angelman Syndrome treated?




There’s no cure for Angelman syndrome. Research focuses on targeting specific genes for treatment. Current treatment focuses on managing medical and developmental issues.


A team of specialists will work with the family or any guardian to manage their child’s condition. Depending on the child’s signs and symptoms, treatment for Angelman syndrome might involve:


  • Anti-seizure medication to control seizures
  • Physical therapy to help with walking and movement problems
  • Communication and speech therapy, which might include sign language and picture communication
  • Behavior therapy to help overcome hyperactivity and a short attention span and to aid in the development
  • Medications and sleep training to manage sleep issues
  • Dietary changes and medications 



How much does Angelman Syndrome treatment cost?




Angelman Syndrome treatment cost starts from $25000, which is one-third of other countries without compromising the treatment quality. India is able to provide the best treatment on a budget because of the low doctor-patient ratio, and various other factors that make India perfect for treatment. 




Contact GoMedii to get the best Angelman Syndrome treatment




If you want Angelman Syndrome treatment in India, choosing GoMedii as your healthcare will be the right choice, as your partner we ensure to make your treatment process hustle-free and affordable. We have partnerships with one of India’s most reputed hospitals that can help you to get the best at an affordable cost, you can contact us on WhatsApp (+91 9599004311) or email us at . Our team will do it. Reply you as soon as possible.




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This Blog Has Been Proofread by Dr. Amit Singh

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