The most common symptoms or signs of Familial Glucocorticoid Deficiency would be very low levels of blood plasma in the body. This is a adrenocortical failure problem that is again hereditary and there is nothing preventive that you can do here. The most common signs of this disease would include skin pigmentation which is often dismissed as something general and not taken seriously.
HOW IS FAMILIAL GLUCOCORTICOID DEFICIENCY DIAGNOSED?
Prenatal diagnosis may be performed in case of family history. Endocrinologists may order for clinical tests that detect the level of serum morning cortisol levels. Genetic testing confirms diagnosis
HOW IS FAMILIAL GLUCOCORTICOID DEFICIENCY TREATED?
The treatment is lifelong with the replacement therapy with oral hydrocortisone. Dose modification is necessary during stresses such as surgery or intercurrent illness, and patients should have injectable hydrocortisone available for emergencies and carry a medical alert type bracelet or card. Prompt and adequate treatment of a hypoglycemic crisis is essential.
DID YOU KNOW?
The treatment for this problem is lifelong and if not monitored correctly, this is a disease that could prove to be fatal in the long run.