Angel syndrome or Williams syndrome is a rare genetic disease with a very low chance of occurrence.
The symptoms may be similar to Down syndrome. Whether it is a symptom related to the child development or the danger of various complications.
Angel disease is caused by
Angel disease is caused by a certain gene on chromosome 7 that is missing since birth. It was found that the symptoms of the disease depend on the missing gene, which may be missing since the egg or sperm. Angel disease can happen to any child, but if both parents have this disease, there may be a 50 percent chance of passing the abnormal trait on to their children.
What are the symptoms of Angel’s Disease?
- Abnormal facial features, such as a small chin, a flat nose, and a mouth that is wider than normal, etc.
- Have learning, language and developmental problems
- Extremely cheerful and can easily get along with strangers. Likes to make loud noises.
- Has low muscle mass and weight since birth.
- Farsightedness, kidney problems, and eating problems
Diagnosis of Angel Disease
- Check blood pressure and measure blood calcium levels.
- Kidney ultrasound examination
- Fluorescent testing involves สมัคร ufabet กับเรา รับโบนัสทันที drawing blood and sending it to a lab for testing so doctors can determine if there are abnormal genes.
- Echocardiography
Complications of Angel’s Disease
- Heart failure due to stenosis
- stomach ache
- Transient hypercalcemia
- When anesthesia is given, it can be life-threatening, but the incidence is very low.
How to treat Angel Disease?
- Practice development in learning, language and speaking.
- Reduce the amount of calcium in the blood by limiting vitamin D.
- Give blood pressure medication
At present, Angel disease cannot be completely cured because it is a genetic disease. Treatment is supported by symptoms. Most children with this disease will be referred to a specialist and will be treated according to the symptoms that occur in the child.
Angel disease, is there a way to prevent it?
Currently, there is no way to prevent this disease. However, if someone in the family has this disease, they should get a diagnosis and consult a doctor before having children to reduce the chance and risk of passing it on to their children.