When Does a Child Need HGH?

When is the appropriate time a child should be treated with Growth Hormone For Kids? Most parents treat them when they notice that their child is shorter than the other kids in as early as 2 years old.

However, some people think that the short stature of the kid is not a problem and may just be genetic, while some think that it may be an underlying disease that causes the child to be short.

Whether if the kid is short but healthy or short and have one or more pediatric conditions, they can be treated with HGH as long as it is approved and prescribed by the doctor.

6 Pediatric Conditions that Needs HGH Treatment

Here are six health conditions of a child that needs a human growth hormone treatment:

  1. Turner Syndrome

This is a chromosomal condition of a female child that affects their development. The most common symptom of this is the short stature that becomes evident at around the age of 5.

Another common symptom of this syndrome is the loss of ovarian function at an early age. A lot of girls do not undergo the stage of puberty unless they are treated. HGH therapy can help treat Turner’s syndrome.

Other symptoms also include nonverbal learning disability, behavioral problems, and developmental delays. These may vary among the affected girls or women.

  1. Growth Hormone Deficiency

This is the most common condition of a child or adult that needs to be treated with GH therapy.

Growth hormone deficiency or GHD occurs when the pituitary gland of the brain doesn’t produce enough growth hormone for the full development of the child’s body. This condition more often affects children than adults.

In 1 out of 7,000 births can acquire a growth hormone deficiency. This can also be one of the symptoms of one of the genetic diseases like Prader-Willi and Turner’s syndrome.

  1. Prader-Willi Syndrome

This one is more complex than the Turner’s syndrome. It is a complicated genetic condition that affects different parts of the body. The symptoms in infants are characterized by poor growth, feeding difficulties, delayed development, and hypotonia or weak muscle tone.

At the beginning of childhood, the affected ones can be insatiable when it comes to eating and can lead them to get obese and have hyperphagia or chronic overeating.

Some people who also have the Prader-Willi syndrome, more particularly the ones with obese can also develop type 2 diabetes. This is the most common form of diabetes.

  1. Noonan Syndrome

This syndrome is caused by the changes in one of the several autosomal of dominant genes. Those who acquire this syndrome might have inherited one of the mutated or altered genes from his or her parents, or the gene change may be due to an error carried by the sperm, occurred, or egg at conception.

This disorder involves short stature, bleeding problems, unusual facial characteristics, malformations of bones of the rib cage, development delays, and heart defects that are present at birth.

  1. Small for Gestational Age

SGA or small for gestational age is the used term to describe a baby that is smaller than the common amount of a number of weeks of pregnancy.

SGA babies may kind of appear neurologically and physically mature, but smaller than other normal babies. SGA babies can also be born prematurely (before 37 weeks), in full term (37 to 41 weeks), or postal term (after 42 weeks).

Some babies may be born small because of genetics, while some may be small because of some fetal growth problems during the pregnancy stage.

  1. Cystic Fibrosis

This genetic disease if progressive that can cause lung infections and limits the individual to breathe properly.

People who have this disease have defective genes that cause a thick and sticky buildup of mucus in the body’s lungs and in other organs. The sticky mucus in the lungs can clog the airways and eventually trap the bacteria leading to an infection, cause lung damage, and in the worst case scenario, cause failure in the respiratory system.

While in the pancreas, the buildup of mucus will prevent the release of digestive enzymes that let the body break down the foods and absorb the nutrients.

There are more of these conditions that can be treated with HGH therapy; these are just one of the most common ones.

Conclusion:

If one or more of the conditions above are present on the current condition of your kid, then take him or her to your family doctor and let them prescribe him or her with an HGH treatment.

The treatment can help prevent further complications and help your child live more comfortably while growing. It may cost you a lot but at least it will give your child a better health.