While these characteristics are helpful in telling one type of diabetes from another, there is considerable overlap making the exact diagnosis difficult and sometimes impossible to decide.
| Typical clinical course |
Usually rapid onset, symptoms for a few weeks to one month |
Usually slower or more subtle onset, symptoms for many months |
| Weight |
Primarily lean, although as more children become overweight, increasing number of children with type 1 are overweight. |
Almost all of the children with type 2 are overweight or obese. |
| Diabetes ketoacidosis (DKA) is diagnosed when the child has ketones in the urine and blood, and is dehydrated and sick. It usually requires hospitalization and IV fluids and insulin. |
This occurs in about 35%-40% of children at the time of diagnosis of type 1. |
A very mild form is found in some children with type 2. It has been reported to occur in type 2 in about 15% of cases at diagnosis. |
| Family history |
5% have a relative with type 1 diabetes
Up to 20% may have a relative with type 2 diabetes
|
Almost all will have at least one relative with type 2. |
| Other conditions in addition to the diabetes |
A host of autoimmune disease such as thyroid and/or adrenal disorders, vitiligo (loss of pigmentation of the skin) and celiac disease are seen in children with type 1 at a higher rate than the general population. Autoimmune disorders also run in family members |
Polycystic ovary syndrome
Acanthosis nigricans (90%)
High Blood Pressure
Other obesity related conditions
|
| C-peptide |
Can be preserved at diagnosis |
Always present |
| Presence of islet auto-antibodies |
Although this is the hallmark of type 1, only 85% of those felt to have type 1 have antibodies. |
Although this is the hallmark of type 1, 15% of those presenting with what looks like type 2 diabetes have antibodies. |