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Table 1 The prevalence of APS1 (n = 13) related components

From: Characterization of the clinical and genetic spectrum of autoimmune polyendocrine syndrome type 1 in Chinese case series

Components

Prevalence (%)

Classic triad

 

 Hypoparathyroidism

12 (92.3)

 Chronic mucocutaneous candidiasis

9 (69.2)

 Addison’s disease

9 (69.2)

 Any of two

5 (38.5)

 All three

6 (46.2)

Other endocrinopathies

 

 Subclinical hypothyroidism

6 (46.1)

 Primary amenorrhea

2 (15.4)

Ectodermal dysplasia

 

 Enamel dysplasia and nail dystrophy

6 (46.1)

 Hair loss

8 (61.5)

Ocular manifestations

 

 Keratitis

1 (7.7)

 Retinitis pigmentation

2 (15.4)

Hematological diseases

 

 Myeloproliferative disease

1 (7.7)

 Pure red cell aplasia

1 (7.7)

Other less common complications

 

 Intestinal malabsorption

3 (23.1)

 Renal tubular acidosis

1 (7.7)

 Asplenia

1 (7.7)

 Autoimmune hepatitis

1 (7.7)

 Ankylosing spondylitis

1 (7.7)

  1. APS1, autoimmune polyendocrine syndrome type 1