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Table 2 Clinical and biochemical features of 42 patients with X-linked AHC

From: Clinical and genetic characteristics of 42 Chinese paediatric patients with X-linked adrenal hypoplasia congenita

 

Infantile-onset (n = 31)

Childhood-onset (n = 11)

P value

 

n (%)

Value

n (%)

Value

Hyperpigmentation

28 (90%)

–

10 (91%)

–

1.0000

Vomiting/diarrhoea

12 (39%)

–

8 (73%)

–

0.0523

Failure to thrive

11 (35%)

–

2 (18%)

–

0.4922

Convulsions

7 (23%)

–

0 (0%)

–

0.2093

Increased ACTH (pg/ml)

31 (100%)

–

11 (100%)

–

–

Decreased cortisol (nmol/L)

27 (87%)

65.1 (22.2–144.1)

10 (91%)

56.0 (19.3–125.0)

0.7565

Hyponatremia (mmol/L)

25 (81%)

125.6 ± 9.3

7 (64%)

129.9 ± 6.9

0.1182

Hyperkalaemia (mmol/L)

23 (74%)

6.3 ± 1.4

6 (55%)

5.1 ± 0.9

0.0033

  1. Values are the means ± standard deviations or medians (interquartile ranges)