Blood sugar levels are abnormally high as the body doesn’t produce enough insulin or the body fails to respond normally to the insulin produced. Weight loss is experienced despite adequate or increased food consumption.
The causes vary depending on genetic makeup, family history, ethnicity, health and environmental factors. The causes of diabetes are undefined as the causes vary depending on the individual and the type.
A hormone that’s released by the pancreas; it allows glucose to move from the blood stream into individual cells. Glucose does not move into the cells and builds up in the blood without a proper amount of insulin. Glucose begins to appear in the urine as glucose levels in the blood increase.
The blood glucose levels are too high to be considered normal. However, it’s not high enough to be considered diabetes. This is common among obese adolescent.
Children with prediabetes are advised to make lifestyle changes. Generally, medication isn’t recommended for children with prediabetes.
This occurs when the pancreas produces too little or no insulin. This is the most common type among children. It’s also as one of the most chronic childhood disease. This may develop any time during childhood or even during birth.
Children with type 1 diabetes take injections of insulin to control blood glucose. Children are usually hospitalized when type 1 diabetes is first diagnosed. They are given fluids (to treat dehydration) and insulin. Since nothing else is effective, they’ll always require insulin.
The cells in the body don’t respond adequately to insulin. The pancreas can still make insulin but not enough to overcome insulin resistance.
Generally untreated in the hospital unless the diabetes is severe. Severe diabetes may require hospitalization to start insulin treatment.
This is common among children with type 1 diabetes; it is one of the most serious immediate complications that can occur. It is present at the time of diagnosis in about one third of children with type 1 diabetes. It also develops in about 1 to 10% of children every year. It is usually because these children have not taken their insulin or are facing problems with insulin delivery.
A diagnosis often follows a person seeking medical advice after experiencing symptoms like:
A blood and urine tests may be ordered to check for high glucose levels to indicate diabetes.
Normal glucose levels range between 4 -7.7 mmol/L or 72-138 mg/dL. The level of blood sugar should always be persistently high as it reflects the body’s inability to use glucose for its various needs.
Thyroid problems are common in overweight children. Hypothyroidism most commonly occurs when the thyroid gland isn’t producing enough thyroid hormone. This could be due to the fact that it won’t produce enough or because it isn’t being stimulated properly.
Children affected are easily spotted because:
Synthetic thyroxine (Levothyroxine) is given to augment the low levels of thyroid hormone (T4). Children who have had longstanding thyroid problem will receive replacement dose slowly over weeks to months in order to avoid unwanted side effects such as:
When the thyroid is too active and releases too much thyroid hormone into the blood stream.
Anti-thyroid drugs are normally given at the start. They have a positive effect after 6 to 8 weeks. There is a much lower likelihood of entering into remission after a course of ATDs than in adults. Radioactive iodine can be used in children in further treatments (especially those aged over 10 years), especially for those whose hyperthyroidism is difficult to control.
An immune-mediated disorder; the thyroid gland overproduces thyroid hormone (hyperthyroidism). It is the most common cause of hyperthyroidism.
Based on the symptoms, age and general health of the child; treatment may be done with:
A rare condition that is associated with a high mortality rate of approximately 20%.
Neonates may suffer from thyrotoxicosis secondary to transplacental transfer of stimulating maternal antibodies. The mothers of these children may either have a history of Graves or they are unaware that they have Graves.
This condition is transient as the maternal antibodies are cleared from the baby’s system by 12 weeks. Even though this is a rare condition, babies with neonatal thyrotoxicosis may have:
Typically, a few days after birth, the babies experience irritability, sweating, vomiting, diarrhoea, tachycardia, poor feeding or hyperthermia and associated hepatomegaly, jaundice or signs of cardiac failure.
This life-threatening condition is managed similarly to the treatment of a thyroid storm. The aims of treatment are to:
These are achieved with a combination of anti-thyroid medication, iodine, steroids and beta-blockers.