Polyendocrine Deficiency
Polyendocrine Deficiency Causes
Many scientists theorize that the polyendocrine deficiency syndrome is inherited. This is mainly because it has been frequently observed that there may be more than one member in the family to have endocrine deficiencies.
Polyendocrine Deficiency Definition
Polyendocrine Deficiency is a disease of which there are two classifications. These are simply called Type I and Type II. This disease is a heterogeneous group of rare disorders represented by autoimmune activity alongside more than one endocrine organ.
Polyendocrine Deficiency Diagnosis
There are different diagnoses depending on the type of polyendocrine deficiency. Like, for example in Type II, antibodies are screened regularly and may lead to hydrocortisone replacement and early intervention to prevent crises.
Polyendocrine Deficiency Symptoms and Signs
Type I: this disorder is an adrenal insufficiency and usually occurs in children. Patients who experience this disorder may also go through under-active parathyroid glands, slow sexual development, pernicious anemia, chronic candida infections, chronic active hepatitis, and, very rarely, hair loss. Type II: also called the Schmidt's syndrome, this disorder troubles young adults. The symptoms may include: an underactive thyroid gland, slow sexual development, diabetes, vitiligo, and pigment loss on areas of the skin.
Polyendocrine Deficiency Treatment
Because of its hereditary nature, there may be no cure. However, the symptoms of this deficiency can be managed with medication. The challenge with this disease is its detection and the anticipation of its manifestations.