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Angelman Syndrome
Treatment of Angelman Syndrome
- Homeopathic Treatment of Angelman Syndrome
- Acupuncture & Acupressure Treatment of Angelman Syndrome
- Psychotherapy Treatment of Angelman Syndrome
- Conventional / Allopathic Treatment of Angelman Syndrome
- Surgical Treatment of Angelman Syndrome
- Dietary & Herbal Treatment of Angelman Syndrome
- Other Treatment of Angelman Syndrome
What is Angelman Syndrome
Symptoms of Angelman Syndrome
Causes of Angelman Syndrome
Risk factors of Angelman Syndrome
Complications of Angelman Syndrome
Lab Investigations and Diagnosis of Angelman Syndrome
Precautions & Prevention of Angelman Syndrome
Treatment of Angelman Syndrome
Homeopathic Treatment of Angelman Syndrome
Homeopathy is safe and natural treatment of neurological conditions. It treats the person as a whole. Treatment is constitutional. It means that homeopathic treatment focuses on the patient as a person, as well as his pathological condition. It balances the energy system, improves immunity and body functions. It naturally cures the root cause of disorder. Some common homeopathic medicines for Angelman syndrome are:
- Agaricus
- Baryta carb
- Cicuta
- Calc P
- Bufo
Acupuncture & Acupressure Treatment of Angelman Syndrome
Acupuncture influences the nervous system by controlling and connecting neuro-physiological relationships between all body systems by directing bio-electrical impulses through the nerve fibers. It also influences the activity of the nerve cells in the spinal cord and brain. The structure and function of the autonomic nerve system and transmissions are controlled by acupuncture treatment.
Psychotherapy Treatment of Angelman Syndrome
Psychotherapy can help children with Angelman syndrome overcome hyperactivity and a short attention span, which can aid in developmental progress.
Conventional / Allopathic Treatment of Angelman Syndrome
Anti-seizure medications may be necessary to control seizures caused by Angelman syndrome.
Dietary & Herbal Treatment of Angelman Syndrome
The Ketogenic Diet is a high-fat diet that carefully controls the amount of carbohydrates (sugars and starches) and proteins that a person with seizures eats.
What is Angelman Syndrome
Angelman syndrome is a complex genetic disorder that primarily affects the nervous system. It causes developmental disabilities and neurological problems, such as difficulty speaking, balancing and walking and, in some cases, seizures.
Symptoms of Angelman Syndrome
- Developmental delays, such as lack of crawling or babbling at 6 to 12 months, and intellectual disability
- Lack of or minimal speech
- Inability to walk, move or balance
- Trembling movement of arms and legs
- Frequent smiling and laughter
- Happy, excitable personality
- Seizures, usually beginning between 2 and 3 years of age
- Stiff or jerky movements
- Small head size, with flatness in the back of the head
- Crossing of the eyes
- Tongue thrusting
- Walking with arms up in the air
- Light pigmentation in hair, skin and eyes
Causes of Angelman Syndrome
- It’s most often caused by problems with a gene located on chromosome 15 called the ubiquitin-protein ligase E3A (UBE3A) gene.
Risk factors of Angelman Syndrome
- Family history of the disease
Complications of Angelman Syndrome
- Abnormal sleep-wake patterns
- Hyperactivity
- Feeding difficulties
- Obesity
- Curving of the spine
Diagnosis of Angelman Syndrome
Diagnosis of Angelman syndrome requires taking a blood sample from your child for genetic studies. A combination of genetic tests can reveal the chromosome defects related to Angelman syndrome. These tests may look at:
- Chromosome size, shape and number
- Missing chromosomes
- Parental DNA pattern
- Gene mutation
Precautions & Prevention of Angelman Syndrome
There is no available prevention for Angelman Syndrome
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