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Racial predominance for APECED Syndrome: Iranian Jews, Sardinian and Finnish populations
Prognosis of APECED Syndrome: The prognosis depends on how well the symptoms are controlled.
Causes of APECED Syndrome: see causes of APECED Syndrome
Symptoms of APECED Syndrome: see symptoms of APECED Syndrome
Onset of APECED Syndrome: Chronic candidiasis is usually the first symptoms and tends to occur within the first 5 years of life. Hypoparathyroidism usually occurs before the age of 10 and adrenal insufficiency usually occurs before the age of 15.
Inheritance:
see inheritance of APECED Syndrome
Treatments for APECED Syndrome:
see treatments for APECED Syndrome
Research for APECED Syndrome:
see research for APECED Syndrome
Main name of condition: APECED Syndrome
Other names or spellings for APECED Syndrome:Autoimmune Polyendocrinopathy [Candidiasis - Ectodermal Dystrophy], Autoimmune Polyglandular Syndrome type I, APS 1
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