Autoimmune Polyendocrine Syndrome

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Types

  • There are two distinct types APS-1 and APS-2
  • APS also named PAS

APS-1

Clinic

  • APS-1 causes the dysfunction of multiple endocrine glands due to autoimmunity.
  • It is an inherited in autosomal recessive fashion


Signs and symptoms

  • Chronic mucocutaneous candidiasis
  • Hypoparathyroidism
  • Addison's disease
  • Ectodermal dystrophy (Skin, Dental enamel, and Nails)


APS-1 may also cause:


APS-1 Entity / Miasm

HSV EBV CMV HCV MMP
Hepatitis +++ +++ +++ +++ +++
Infertitiy +++ +++
Vitiligo +++ +++
Atrophic Gastritis +++ +++
Cataract +
Cerebellar ataxia +++ +++ +++
Autoimmune adrenalitis ++ + +++
Alopecia +


APS-2

Clinic

  • It is the most common form
  • It is heterogeneous and has not been linked to one gene.
  • It affects women to a greater degree than men.


Signs / Symptoms

  • Hashimoto thyroiditis: Nausea, Frequent urination, Palpitations, Weight loss, Anorexia
  • Low blood pressure
  • Hypoparathyroidism
  • Myalgia
  • Graves' disease
  • Anemia
  • Hypogonadism
  • Diabetes mellitus


APS-2 Entities / Miasms

MTB MMP EBV HCV
Infertility +++ +++
Hashimoto thyroiditis +++ +++ +++ +++
Anemia +++ +++ +++
Diabetes mellitus, juvenile +++


Note

It seems that APS is a COE.