Human Growth Hormone is highly useful in many medical situations.
While it is commonly used by the public for purposes which have not been approved by the FDA, it also has many on-label, or approved, uses.
Most of these approved uses are for medical issues which result in a smaller than normal stature. The Human Growth Hormone supplementation helps the individual to reach or maintain a normal stature for their gender and age.
HGH Deficiency or Insufficiency
Human Growth Hormone is an approved treatment plan for children who are experiencing HGH deficiency or insufficiency.
This is generally caused by an underactive pituitary gland. Supplementing their low Human Growth Hormone levels with synthetically made HGH allows such children to achieve a normal stature once they are an adult. Many children who undergo this treatment will experience delayed puberty, but this is a small price to for most of them.
Turner’s syndrome is a disease which affects only women; scientifically speaking, it occurs when a female has only one X chromosome rather than the typical two.
This can lead to a host of problems, including but not limited to developmental abnormality and infertility.
Many Turner’s females experience a wide variety of symptoms linked with their disorder, such as a short stature, swelling of the hands and feet, small fingernails, lack of a menstrual period, and a broad chest.
Human Growth Hormone is often prescribed to those females with Turner’s syndrome suffering from short stature; this will often help them reach an appropriate height by the time they are finished growing.
Short Bowel Syndrome
Unlike the other disorders listed here, short bowel syndrome, also known as short gut syndrome, is often the result of something that occurs during one’s lifetime rather than something one is born with.
It is often the result of surgery, particularly in individuals who have preexisting bowel disorders like Crohn’s disease or Irritable Bowel Syndrome.
Short bowel syndrome is characterized by absorption issues which often lead to the individual having to obtain their nutrition intravenously.
Some of these individuals have been prescribed Human Growth Hormone and have seen good results. Many of these patients have experienced a decreased need for intravenous supplementation while taking Human Growth Hormone.
Unlike short bowel syndrome, Prader-Willi syndrome is present in individuals from birth onwards.
This disorder affects multiple parts of the body and is characterized by such symptoms as obesity, reduced mental faculties and abilities, reduced muscle tone, an insatiable appetite, and sex glands which produce little to no sex hormones.
Prader-Willi syndrome patients who have been treated with Human Growth Hormone often see a reduction in these symptoms.
The doses of growth hormone given to them help the body produce more of the hormones needed for necessary function and patients often see a reduction in fat-derived weight and an increase in lean muscle.
Children with Prader-Willi syndrome who are given Human Growth Hormone should be closely monitored lest they develop glucose intolerance. At home monitoring for this complication can be done using urine glucose dipsticks.