Short stature
A diagnosis of restricted growth (dwarfism)is based on symptoms, height measurements, family history and tests.
Depending on the cause of the condition, restricted growth may be diagnosed before or soon after a child is born, or when growth problems become more obvious as they get older.
Tests may not need to be carried out if you or your child dont have any other health problems.
Growth hormone deficiencyis usually diagnosed using growth hormone stimulation tests.
Medicine isinjected into a vein to cause growth hormone levels in the bloodto increase. If the level of growth hormone is found to be lower than normal, it indicates growth hormone deficiency.
A scan of the brain is necessary to look at the pituitary gland (which produces growth hormone) if blood tests showlow levels ofgrowth hormone.
The following testscan beused to diagnose a condition thatcauses short stature:
Diagnosis during pregnancy (also called prenatal diagnosis) may be offered to parents who have a genetic history of a condition that causes short stature.
Some potential abnormalities may be visible during routine ultrasound scans ,but tests such as chorionic villus sampling or amniocentesis are needed to confirm a diagnosis,as they can be used to seeif your baby carries one of the faulty genes associated with restricted growth.
Restricted growth, sometimes known as dwarfism, is a condition characterised by short stature.
People with restricted growth (dwarfism) often have no symptoms other than short stature, although some people have associated health problems.
Restricted growth (dwarfism) may be caused by many different medical conditions, and is more noticeable in some conditions than others.
A diagnosis of restricted growth (dwarfism) is based on symptoms, height measurements, family history and tests.
Some people with restricted growth may be able to have treatment to help them grow more than they otherwise would, although not everyone will need treatment.