Short Stature (Growth Disorders) Overview
Learn About Short Stature (Growth Disorders)
A child who has short stature is much shorter than children who are the same age and sex.
Your health care provider will go over your child’s growth chart with you. A child with short stature’s height is:
- Two standard deviations (SD) or more below the average height for children of the same sex and age.
- Below the 2.3rd percentile on the growth chart: Out of 1,000 boys (or girls) who were born on the same day, 977 of the children are taller than your son or daughter.
Your child’s provider checks how your child is growing at regular checkups. The provider will:
- Record your child’s height and weight on a growth chart.
- Monitor your child’s growth rate over time. Ask the provider what percentile your child is for height and weight.
- Compare your child’s height and weight to other children of the same age and sex.
- Talk with you if you are worried that your child is shorter than other children. If your child has short stature, this does not necessarily mean that something is wrong.
Common conditions include: Achondroplasia, Familial Short Stature (FSS), Growth Hormone Deficiency (GHD), Idiopathic Short Stature (ISS)
There are many reasons why your child has short stature.
Most of the time, there is no medical cause for short stature.
- Your child may be small for her age, but is growing OK. She will probably start puberty later than her friends. Your child will most likely keep growing after most of her peers have stopped growing, and will probably be as tall as her parents. Providers call this “constitutional growth delay.”
- If one or both parents are short, your child will most likely also be short. Your child should get as tall as one of her parents.
Sometimes, short stature may be a symptom of a medical condition.
Bone or skeletal disorders, such as:
- Rickets
- Achondroplasia
Long-term (chronic) diseases, such as:
- Asthma
- Celiac disease
- Congenital heart disease
- Cushing disease
- Diabetes
- Hypothyroidism
- Inflammatory bowel disease
- Juvenile rheumatoid arthritis
- Kidney disease
- Sickle cell anemia
- Thalassemia
Genetic conditions, such as:
- Down syndrome
- Noonan syndrome
- Russell-Silver syndrome
- Turner syndrome
- Williams syndrome
Other reasons include:
- Growth hormone deficiency
- Infections of the developing baby before birth
- Malnutrition
- Poor growth of a baby while in the womb (intrauterine growth restriction) or small for gestational age
This list does not include every possible cause of short stature.
Contact your provider if your child appears to be much shorter than most children their age, or if they seem to have stopped growing.
The provider will perform a physical exam. The provider will measure your child’s height, weight, and arm and leg lengths.
To figure out possible causes of your child’s short stature, the provider will ask about your child’s history.
If your child’s short stature may be due to a medical condition, your child will need lab tests and x-rays.
Bone age x-rays are most often taken of the left wrist or hand. The provider looks at the x-ray to see if the size and shape of your child’s bones have grown normally. If the bones have not grown as expected for your child’s age, the provider will talk more about why your child may not be growing normally.
Your child may have other tests if another medical condition may be involved, including:
- Complete blood count
- Growth hormone stimulation
- Thyroid function tests
- Insulin growth factor-1 (IGF-1) level
- Blood tests to look for liver, kidney, thyroid, immune system, and other medical problems
Your provider keeps records of your child’s height and weight. Keep your own records, too. Bring these records to your provider’s attention if the growth seems slow or your child seems small.
Your child’s short stature may affect their self-esteem.
- Check in with your child about relationships with friends and classmates. Kids tease each other about many things, including height.
- Give your child emotional support.
- Help family, friends, and teachers emphasize your child’s skills and strengths.
TREATMENT WITH GROWTH HORMONE INJECTIONS
If your child has no or low levels of growth hormone, your provider may talk about treatment with growth hormone injections.
Most children have normal growth hormone levels and will not need growth hormone injections. If your child is a boy with short stature and delayed puberty, your provider may talk about using testosterone injections to jump-start growth. But this is not likely to increase adult height.
Reviewed By: Neil K. Kaneshiro, MD, MHA, Clinical Professor of Pediatrics, University of Washington School of Medicine, Seattle, WA. Also reviewed by David Zieve, MD, MHA, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.
Review Date: August 10, 2021.
University Of Arkansas For Medical Sciences
Donald Bodenner is an Endocrinologist in Little Rock, Arkansas. Dr. Bodenner and is rated as an Advanced provider by MediFind in the treatment of Short Stature (Growth Disorders). His top areas of expertise are Thyroid Cancer, Hyperparathyroidism, Thyroid Nodule, Thyroidectomy, and Parathyroidectomy.
Northeast Arkansas Clinic Charitable Foundation, Inc.
Kevin Ganong is an Endocrinologist in Jonesboro, Arkansas. Dr. Ganong and is rated as an Experienced provider by MediFind in the treatment of Short Stature (Growth Disorders). His top areas of expertise are Thyroid Storm, Thyroid Nodule, Hyperparathyroidism, and Type 1 Diabetes (T1D).
St Vincent Medical Group
Allen Redding is an Endocrinologist in Little Rock, Arkansas. Dr. Redding and is rated as an Advanced provider by MediFind in the treatment of Short Stature (Growth Disorders). His top areas of expertise are Type 2 Diabetes (T2D), Thyroid Storm, Familial Hyperaldosteronism, and Hyperaldosteronism.
Summary: The purpose of this study is to evaluate i) the effect of multiple doses of vosoritide and ii) the effect of the therapeutic dose of vosoritide compared to human growth hormone (hGH), in children with idiopathic short stature (ISS).
Summary: The purpose of this basket study in children with Turner syndrome, SHOX deficiency, and Noonan syndrome is to evaluate the effect of 3 doses of vosoritide versus hGH on growth as measured by AGV after 6 months of treatment. The long-term efficacy and safety of vosoritide at the therapeutic dose will be evaluated up to FAH.