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Alternative Names Return to top
Panhypopituitarism; Dwarfism; Pituitary dwarfismDefinition Return to top
Growth hormone deficiency involves abnormally short stature with normal body proportions. Growth hormone deficiency can be categorized as either congenital (present at birth) or acquired.
Causes Return to top
An abnormally short height in childhood may occur if the pituitary gland does not produce enough growth hormone. It can be caused by a variety of genetic mutations (such as Pit-1 gene, Prop-1 gene, growth hormone receptor gene, growth hormone gene), absence of the pituitary gland, or severe brain injury, but in most cases no underlying cause of the deficiency is found.
Growth retardation may become evident in infancy and persist throughout childhood. The child's "growth curve," which is usually plotted on a standardized growth chart by the pediatrician, may range from flat (no growth) to very shallow (minimal growth). Normal puberty may or may not occur, depending on the degree to which the pituitary can produce adequate hormone levels other than growth hormone.
Growth hormone deficiency may be associated with deficiencies of other hormones, including the following:
Physical defects of the face and skull can also be associated with abnormalities of the pituitary or pituitary function. A small percentage of infants with cleft lip and cleft palate have decreased growth hormone levels.
Symptoms Return to top
Exams and Tests Return to top
A physical examination including weight, height, and body proportions will show signs of slowed growth rate and deviation from normal growth curves.
Tests may include the following:
Treatment Return to top
Synthetic growth hormone can be used for children with growth hormone deficiency. This treatment requires the assistance of a pediatric endocrinologist. Treatment with synthetic (recombinant) human growth hormone is generally considered to be safe, with rare side effects.
If the deficiency is an isolated growth hormone deficiency, synthetic growth hormone is given alone. If the deficiency is not isolated, other hormone replacement preparations will be required as well.
Outlook (Prognosis) Return to top
Growth rates are improved in most children treated with growth hormones, although the effectiveness may decrease with prolonged treatment.
Possible Complications Return to top
If left untreated, extremely short stature and delayed puberty will result from this condition.
In the past, some patients acquired Creutzfeldt-Jacob disease (the human form of "mad cow" disease) from human-derived growth hormone that was used to treat growth deficiencies. This medication has been removed from the market.
Synthetic growth hormone is used instead and carries no risk of infectious disease.
When to Contact a Medical Professional Return to top
Call your health care provider if your child seems abnormally short for his or her age.
Prevention Return to top
Most cases are not preventable.
Review your child's growth chart with your physician after each check up. If you child's growth rate is dropping or your child's projected adult height is much shorter than an average height of both parents, evaluation by a specialist is recommended.
Adjusted average height of both parents is as follows:
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Page last updated: 02 January 2008 |