Down syndrome are most common in babies 

What is Down syndrome?

A hereditary health disorder as Down syndrome is a chromosomal defect happens in various people which cause:

  • Cerebral Disability
  • Cognitive Disabilities
  • Physical Growth Holds-Up
  • Attribute Facial Features
  • Digestive Problems Such As Obstruction Of Intestines
  • Heart Defects
  • Hearing Or Vision Problems
  • Thyroid Issues (Specially, Hypothyroidism, Which Affects About 15% Of The Down Syndrome Patients)

However, these disabilities last permanent and can also warn life expectancy. Though, today with hi-tech and advancement in medical science, strong networks, and more consideration of this disorder people with Down syndrome along with their families can effectively find the way through the challenges caused by this condition. You can booking for doctors for prescription and discussion using 1mg Coupons available to get free appointments.

What are the symptoms of Down syndrome? 

People with Down syndrome show different physical features such as:

  • Short neck which also seems relatively flat with surplus skin at the back
  • Eyes incline upwards a little and are almond formed
  • The external part of the iris in the eyes might have light spots that are known as brushfield spots
  • Bridge of the nose is small which provides the feeling of a key and big nose
  • Small ears and head
  • Firmed facial profile
  • Short and plump fingers
  • Short hands
  • Low and poor muscle tone which affects all the muscles in the body
  • A breach between the big toe and the rest of the toes
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The cognitive and behavioural symptoms comprise:

  • Problems with thoughts
  • Less focus span
  • Poor decision making
  • Spontaneous behavior
  • Slow learning
  • Deferred language and speech development

down syndrome

  • Vision loss
  • Hearing issues
  • Digestive problems such as obstruction of intestines
  • Heart defects
  • Thyroid problems (hypothyroidism, which affects around 15% of the down syndrome patients)
  • Common infections due to problems in the immune system

Blood disorders (children with down syndrome are much more expected to have leukemia)

    • Hearing issues
    • Digestive problems such as obstruction of intestines
    • Heart defects
    • Thyroid problems (hypothyroidism, which affects around 15% of the down syndrome patients)
    • Common infections due to problems in the immune system
  • Obstreperous sleep apnea
  • Gum diseases
  • Epilepsy
  • Mind health and emotional problems
  • Celiac disease
  • Some children might suffer from distorted bones in the upper part of the backbone

How is Down syndrome diagnosed?

Doctors can treat Down syndrome during pregnancy or after delivery of child. The following tests are generally recommended by specialists:

  • Prenatal tests: These tests include:
  • Blood tests
  • Ultrasound
  • Combination of blood tests and ultrasound

These tests are applied throughout the first and second trimester of pregnancy and are screening tests, which can assess the threat of having a baby with Down syndrome. The tests cannot make sure show whether your baby has or does not have Down’s syndrome. They can just show how high your threat is.

There are diagnostic tests such as:


With this test, a sample of your amniotic liquid is tired by using a needle which is putting into your uterus. This sample test is done for the more chromosomes which cause Down syndrome. This test is mainly done after 15 weeks of pregnancy. The threat of miscarriage linked with this test is very low.

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Chorionic villus sampling (CVS):

 With this test, some cells are picked from your placenta and transferred to the lab to test the fetal chromosomes and detect if there is an additional chromosome. This test is done usually between 10 and 13 weeks of pregnancy and the threat of miscarriage related with this test is very low.


Chromosomal testing of maternal blood:

 This test is done by taking blood from a pregnant woman and doing a chromosomal test which might find out the additional chromosome, as the mother’s blood holds the DNA of the fetus. 

Diagnosis after birth:

 Diagnosis of Down syndrome test is performed after the delivery of child by mother and it is based on the physical look of the baby and a blood test which is performed to check out the child’s chromosomes.

What is the treatment of Down syndrome?

Medical Treatment for Down Syndrome 

Early involvement is necessary for Down syndrome from the time when people are undergoing from this disorder are at a bigger risk of going through from different health problems than people who do not undergo from this disorder. However, most of the related disorders might need medical intrusion just after child birth, during teenage years right into maturity. 

For example, an infant born with Down syndrome might need a heart surgery right away after birth if he/she is born with a heart failing. Or if the infant experiences from any specific digestive troubles he/she might require taking a particular way of diet fixed with the required treatment. Just avail updates on Freejobalert by just subscribing free of cost.


Researches show that people suffering from Down syndrome are less prone to do exercise for the most part due to low muscle tone. However, they look to have less ability for cardiovascular and muscular work-outs.  

However, existing statistics also indicates that doing exercise every day is more advantageous for slowly growing the exercise capability and physiological functions in people with Down syndrome. 

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