While some pediatric endocrine disorders can be easily diagnosed, others may be trickier to detect. Common pediatric endocrine disorders include short stature, Turner syndrome, type 1 diabetes, and thyroid disorders.

Often, these disorders may impact linear growth, behavior, cognition or school performance, energy levels, and/or hasten or delay pubertal development. For these reasons, it is important to diagnose pediatric endocrine disorders early on and start treatment promptly.

In this blog, we will discuss the signs, symptoms, and treatments for common pediatric endocrine disorders.

Short Stature and Abnormal Linear Growth

pediatric endocrine disorders of short stature

Short stature can be defined as being less than the third percentile on the growth curve or significant short stature as below the first percentile. Abnormal linear growth happens when a child starts crossing growth percentiles. The latter is most concerning, but both should be given some thought and evaluation.

Evaluating & Treating Short Stature

An evaluation would include a medical provider asking specific questions related to general health, obtaining family history, familial heights, current medications, and performing a thorough physical exam. A bone age is determined with an x-ray of the left hand looking at growth plates and bone maturation. Blood work might also be warranted to look for an etiology.

Qualifying children may be eligible for treatment with recombinant growth hormone injections. These children will often be referred to a Pediatric Endocrinologist for further evaluation and initiation of growth hormone therapy. Extremely short children benefit most from growth hormone therapy when it’s initiated early and before they start puberty.

Turner Syndrome

Turner syndrome is a genetic condition where girls are missing an X chromosome in some or most of the cellsTurner syndrome can be suspected in utero on a prenatal ultrasound, soon after birth or during adolescense if physical signs are subtle.  Prenatal genetic testing can aid in early diagnosis.

Signs of Turner Syndrome

Some signs and symptoms of Turner syndrome include:

  • Puffy hands and feet
  • Wide neck
  • Slowed growth/short stature
  • Heart malformation
  • Delayed puberty
  • Abnormal kidneys

Diagnosis and Treatment of Turner Syndrome

Often the primary care team will order a karyotype to confirm the diagnosis. After the diagnosis is made, many tests and studies, if not already done, are conducted to look for associated features.

Treatment will depend on the findings of the tests and studies. A pediatric endocrinologist is often an essential member of the care team for children with Turner syndrome. In fact, a pediatric endocrinologist may see your child more often than her primary care provider.

Girls with Turner syndrome see a pediatric endocrinologist specifically for slowed growth or pubertal delays and autoimmune diseases such as hypothyroidism, hyperthyroidism, or type 1 diabetes. As slowed growth becomes obvious, often recombinant growth hormone is initiated to improve adult height outcomes. It is beneficial to start treatment as soon as slowed growth is observed to get the maximum benefit from growth hormone.

Another aspect of treatment provided by a pediatric endocrinologist is pubertal initiation. More often than not, girls with Turner syndrome do not start puberty. Not only is estrogen vital for bone health, cardiovascular health, and the adolescent growth spurt, it is important for these girls to experience similar changes seen in puberty as their peers.

Type 1 Diabetes

Type 1 Diabetes is an autoimmune condition in which the immune system destroys the cells that make insulin. Insulin is a hormone that allows the cells in the body to use glucose as a fuel source. Without insulin, glucose levels are high in the bloodstream and in the urine. The body starts to use fat as energy alternatively leading to the build of ketones in the bloodstream and urine that  worsen the severity of the illness.

Signs of Type 1 Diabetes

Some signs and symptoms of Type 1 diabetes include:

  • Weight loss
  • Nausea/vomiting
  • Thirst
  • Abdominal pain
  • Frequent urination
  • Vision changes
  • Hunger
  • Fatigue

Diagnosis & Treatment of Type 1 Diabetes

The diagnosis of type 1 diabetes is made from blood work. Elevated blood glucose levels are noted and there may also be presence of ketone bodies in the blood and urine. Antibody levels are often measured to confirm the diagnosis of type 1 diabetes.

The treatment involves prompt initiation of insulin injection therapy. Soon after the child is diagnosed with type 1 diabetes, a pediatric endocrinologist is consulted. Moreover, the pediatric endocrinologist will make recommendations on insulin therapy and doses. The family and child are taught how to manage diabetes at home.

Your child may also be a candidate for immunotherapy to delay the onset of Type 1 Diabetes.

The child will see the pediatric endocrinologist every 3 months or more frequently if needed. If the diagnosis is delayed, the child may present severely ill and require admission to the intensive care unit and placed on intravenous insulin.

Graves' Disease

Graves' disease is an autoimmune disease that leads to an overactive thyroid gland or hyperthyroidism. It is the most common cause of hyperthyroidism in children.

Signs of Graves' Disease

Here are some signs and symptoms of Graves' disease:

  • Enlarged thyroid gland
  • Difficulty sleeping
  • Bulging eyes
  • Weight loss
  • Poor school performance
  • Menstrual irregularities
  • Fidgeting
  • Nervousness
  • Increased appetite
  • High heart rate

Diagnosis & Treatment of Graves' Disease

For Graves' Disease, the diagnosis is made by evaluating thyroid hormone levels in the blood. There are several treatment options available after discussion with your pediatric endocrinologist based on the clinical findings and the age of the child.

A common therapy is to give medication that lowers the thyroid hormones that are released from the thyroid gland. The other option is to give radioactive iodine to ablate or destroy the gland. Some individuals might be better suited for surgical removal of the thyroid gland.

Early diagnosis and treatment are important to help the child feel better, grow normally, and improve school performance if impacted.

Hashimoto’s Thyroiditis

Hashimoto’s thyroiditis is an autoimmune condition that can lead to hypothyroidism or an under active thyroid gland. It is the most common cause of hypothyroidism.

In this condition, the immune system destroys the thyroid gland.  During this immune dysregulation, there may be a transient hyperthyroid phase as thyroid hormone is released freely.  Some individuals will end up needing thyroid hormone replacement.

Signs of Hashimoto's Thyroiditis

hashimoto's disease

Here are some signs of Hashimoto’s hypothyroidism:

  • Goiter
  • Delayed puberty
  • Slowed growth
  • Constipation
  • Decreased heart rate
  • Fatigue

Diagnosis & Treatment of Hashimoto's

In order to diagnose Hashimoto's, obtaining blood levels of thyroid hormones is necessary.

Pediatric endocrinologists often are consulted to manage a child with hypothyroidism. Usually, treatment involves providing thyroid hormone tablets. It is important to treat hypothyroidism early to help the child feel better, grow normally, and normalize metabolism.

Congenital Hypothyroidism

Congenital hypothyroidism is a condition where a baby has hypothyroidism or under active thyroid gland. In most cases, it arises from an abnormal formation or lack of formation of the thyroid gland.

In the United States, neonates are diagnosed based on mandated newborn screening. This is because most infants are not symptomatic, and treatment prevents neurocognitive delays.

Signs of Congenital Hypothyroidism

While most infants tend not to show symptoms, here are some signs and symptoms of congenital hypothyroidism:

  • Constipation
  • Enlarged tongue
  • Slow growth
  • Prolonged jaundice
  • Low heart rate
  • Poor feeding
  • Low body temperature

Diagnosis and Treatment of Congenital Hypothyroidism

Infants who are diagnosed by newborn screening methods will have confirmatory blood work. They will often be referred to a pediatric endocrinologist for ongoing management. It is very important to start treatment and normalize thyroid hormone levels, so the infant’s brain development is not harmed.

Find the Right Pediatric Endocrinologist for Your Child

These disorders, if left untreated, can have serious long-term consequences for a child's growth and development. However, with early detection and proper treatment, many children with endocrine disorders can lead healthy and normal lives.

It is crucial for parents and healthcare providers to be aware of the signs and symptoms of these disorders and to seek medical attention promptly if they suspect their child may be affected. By working together, we can ensure that every child receives the best possible care and support for their endocrine health.

For more information about pediatric endocrine disorders and how to get the best treatment, follow our blog or contact Dr. McIver.

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Short Stature

How is short stature syndrome in childhood defined? Based on population norms, a child is short when the height percentile is below the 3rd percentile.  In children younger than two years old, the child is plotted on the World Health Organization or WHO growth curves.  After the age of two and when the child can stand for a height measurement, the Center of Disease Control or CDC growth curves are used.  

A short child does not necessarily mean an unhealthy child.  If a child is consistently growing at the 3rd percentile with appropriate weight gain this could be considered appropriate.  If child was growing at the 50th percentile and then starts to cross growth percentiles, then this child deserves some evaluation.

We often look at the childs height in relationship to the mid-parental height.  The mid-parental height is a calculation based on the parent’s height. 

Calculations are in inches.
For a boy:  
Mid-parental height=(mom’s height +5 plus dad’s height)/2

For a girl:
Mid-parental height=(dad’s height -5 plus mom’s height)/2

The genetic potential is +/-3 inches.

If the childs height percentile is within this genetic height potential then this is considered to be appropriate for that child.  

If the child is below this window, your child’s PCM may do further evaluation or monitor the growth especially if its tracking.  If there are concerns, a work up is initiated and referral may be sent to endocrinology, genetics, and/or gastroenterology.

https://www.cdc.gov/growthcharts/background.htm

https://www.cdc.gov/growthcharts/who_charts.htm

What are thyroid antibodies?  Thyroid antibodies can be evaluated for by a blood test. Two such antibodies are anti thyroid peroxidase antibody (TPO Ab) and anti-thyroglobulin antibody (antiTg Ab).   Most commonly TPOAb levels are evaluated in individuals with hypothyroidism.

What does it mean when TPOAb are positive? Upto 20% of the population may have positive TPOAb and have normal thyroid function.  Having positive thyroid antibodies may increase the risk for developing thyroid dysfunction over time.  However, you may have positive antibodies and not develop thyroid dysfunction or need medication.  Positive thyroid antibodies are seen in autoimmune thyroid disease which include Hashimoto’s and Graves disease.

What is Hashimoto’s disease? It has other names such as chronic lymphocytic thyroiditis, or autoimmune thyroiditis.  This is a condition where there is autoimmune destruction of the thyroid tissue leading to hypothyroidism or an underactive thyroid gland.  Majority of individuals with Hashimoto’s disease will have positive TPOAb and anti-TgAb.  In this condition, if enough thyroid gland destruction occurs, thyroid hormone replacement is needed to maintain normal thyroid levels in the blood.  

What is Graves disease?  Graves disease is an autoimmune condition that leads to an overproduction of thyroid hormones or hyperthyroidism.  Individuals with this condition may have difficulty gaining weight, sleep disturbances, heat intolerance/sweating, increased appetite, increased bowel movements, increased heart rate and blood pressure along with eye disease.  They can have positive TPOAb but also have antibodies that stimulate the TSH receptors on the thyroid cell or thyrocyte.

https://www.niddk.nih.gov/health-information/endocrine-diseases/hashimotos-disease

https://www.mayoclinic.org/thyroid-disease/expert-answers/faq-20058114#:~:text=The%20presence%20of%20TPO%20antibodies,that%20mistakenly%20attack%20normal%20tissue

What is non-thyroidal illness or sick euthyroid syndrome?

The simplest way to explain is that when the body in under tremendous stress, it reduces the amount of thyroid hormone produced.  Typically, under these conditions thyroid hormone replacement is not provided and once the stress is gone, the thyroid hormone production rebounds back to normal.

This can be seen is children who are in the intensive care unit or even those who had a recent viral infection.  It is important to repeat blood work in these cases once the illness is resolved to show that the thyroid hormone production has normalized.

New Treatment to Delay Type 1 Diabetes

On November 17,2022 the FDA approved a new treatment to delay the onset of type 1 Diabetes in those over 8 years of age and those who are at high risk for developing diabetes.  The drug is called teplizumab and its an anti-CD3 monoclonal antibody.  

Those that qualify need to have positive diabetes autoimmune antibodies and start to show glucose irregularities without overt symptoms.  This is referred to stage 2 diabetes.  To learn more about the other stages click on this hyperlink https://www.trialnet.org/t1d-facts

The drug interferes with autoimmune destruction of the pancreatic cells that make insulin.  Insulin is needed to keep blood sugars tightly controlled.

Though this is not a cure for diabetes, its a huge milestone in the treatment/care of diabetes and it could delay the onset of type 1 diabetes by 2 years.

https://www.trialnet.org/our-research/completed-studies/teplizumab

 
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Importance of Thyroid Hormone

Why are thyroid hormones so important?

Thyroid hormone is important for many organs of the body.  It is crucial for brain development in the those less than 2 years of age.  Untreated thyroid hormone deficiency in this age group leads to irreversible cognitive delays.  In addition, thyroid hormone is involved in the body’s metabolism from heart rate, the pace of food is processed and absorbed, body temperature, and impacts how the liver functions.  It can also impact muscle function and in childhood lead to delays in achieving gross motor milestones such as walking.  Lack of thyroid hormone can also delay puberty, cause menstrual irregularities, and lead to abnormal growth.

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HPT Axis

What is the Hypothalamic-Pituitary-Thyroidal (HPT) Axis?

Thyroid hormones are tightly regulated in the body.  There is a feedback loop that keeps hormones at appropriate levels as depicted in the diagram below.

The hypothalamus and pituitary release just the right amount of hormones that stimulate the thyroid gland to release thyroxine (T4) and triiodothyronine (T3). The thyroid gland releases mostly thyroxine which gets converted into the active form of thyroid hormone.

There are thyroid hormone receptors or sensors on the hypothalamus and pituitary that then downregulate the thyroid from releasing too much hormone.

Once the diagnosis of hypothyroidism is made, medication is initiated.  Typically levothyroxine in the form of a tablet is provided.  There are liquid formulations but they often tend to be expensive.  Tablets are just as effective and can be easily crushed for young patients who cannot chew or swallow them. 

Levothyroxine is typically given on an empty stomach.  However, in infants who are feeding frequently this is not possible.  For this population, the important thing is being consistent with when the medication is provided.  It is best to avoid supplements such as iron and calcium for at least 4 hours as they tend to impair the absorption of the medication.  Simethicone, antacids, and soy products also impact the absorption.  It is also recommended not to crush the tablet and place into a baby’s bottle.  There are two reasons for this.  One there is concern that the infant will not finish the bottle and two, the medication has an affinity for plastic. 

If a dose is missed at the usual scheduled time, the dose can be provided when the parent remembers later in the day.  The dose can also be doubled the next day.  

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Hashimotos vs Hypothyroidism

Hashimoto's disease is not the same as hypothyroidism.  Hashimoto's disease is an autoimmune condition in which there is inflammation of the thyroid gland.  It is also referred to as chronic lymphocytic thyroiditis.  In this condition, the immune system attacks and destroys thyroid tissue.  During this destructive phase, an individual can experience transient hyperthyroidism where the thyroid cells release thyroid hormone in an unregulated manner. Hyperthyroidism is when the gland is overactive and produces more thyroid hormones than are needed.  This phase, if it were to occur, is referred to as hashitoxicosis.  Once enough tissue has been destroyed, hypothyroidism will occur.  Blood work most likley with detect postivie antibodies and abnormal thyroid hormone values.  If an ultrasound is obtained, the thyroid gland maybe enlarged, show increased blood flow, and appear to have pseudonodules giving the gland a giraffe-like pattern.  Overtime, if the gland has been destroyed it will appear atrophic or small with decreased blood flow.  Of note, an ultrasound is not required to make the diagnosis nor needed for routine management.

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DIET AND HYPOTHYROIDISM

There is no proven diet for hypothyroidism that would aid in the treatment or cure.  Acquired hypothyroidism due to autoimmune dysregulation is associated with other autoimmune disorders such as celiac disease.  In this case, a gluten free diet is recommended. 

There are important micronutrients that are required for normal thyroid function such as iodine and selenium.   It is important to eat a well balanced diet to get the proper nutrients for normal function in the body.   Iodine deficiency is the most common cause of hypothyroidism in developing countries but not in the United States.  Selenium also plays an important role in thyroid function.  There is some literature that supports that selenium supplements may reduce autoimmune markers in thyroid disease but it is not clear how this improves the course or outcomes of hypothyroidism.  On the other hand taking too much iodine or selenium supplements can cause adverse health outcomes as well.

Recommended Dietary Reference Intakes (The Harriet Lane Handbook, 20th ed.)

 

Iodine mcg/d

Selenium mcg/d

0-6 mo

110

15

7-12 mo

130

20

1-3 yr

90

20

4-8 yr

90

30

9-13 yr

120

40

14 yr and up

150

55

Hu S, Rayman MP. Multiple Nutritional Factors and the Risk of Hashimoto's Thyroiditis. Thyroid. 2017 May;27(5):597-610. doi: 10.1089/thy.2016.0635. Epub 2017 Apr 6. PMID: 28290237.

Ventura, M., Melo, M., & Carrilho, F. (2016). Selenium and Thyroid Disease: From Pathophysiology to Treatment. International Journal of Endocrinology, 2017. https://doi.org/10.1155/2017/1297658

Gorini F, Sabatino L, Pingitore A, Vassalle C. Selenium: An Element of Life Essential for Thyroid Function. Molecules. 2021 Nov 23;26(23):7084. doi: 10.3390/molecules26237084. PMID: 34885664; PMCID: PMC8658851.

Winther K, H, Papini E, Attanasio R, Negro R, Hegedüs L: A 2018 European Thyroid Association Survey on the Use of Selenium Supplementation in Hashimoto’s Thyroiditis. Eur Thyroid J 2020;9:99-105. doi: 10.1159/000504781