Table 1.

Diagnoses of included patients (n  = 180).

Adrenal	n	Thyroid	n	Gonads	n	Pituitary	n	Other	n
Addison’s disease	8	Graves’ disease	6	Oligo-/amenorrhoea	4	Congenital pituitary anomaly	15	Polyglandular syndrome	1
17a-OH hydroxylase deficiency	1	Congenital hypothyroidism	6	Complete androgen insensitivity syndrome (CAIS)	4	(Pan) hypopituitarism	4	Fanconi anaemia	2
Hyperandrogenism	1	Multinodular goitre	2	Polycystic ovary syndrome (PCOS)	9	Central adrenal insufficiency	1	Follow-up after (chemo-)radiation	25
Congenital adrenal hyperplasia (CAH) salt loosing type	9	Hemi- or total thyroidectomy	3	Sex chromosome mosaicism	2	Diabetes insipidus	4	Hypophosphatemic rickets	2
Congenital adrenal hyperplasia (CAH), non-salt loosing type	4	Hashimoto thyroiditis	2	Hypogonadotropic hypogonadism	3	Growth hormone deficiency	2	McCune-Albright syndrome	1
DAX1 gene mutation	1	Toxic thyroid adenoma	1	Kallmann syndrome	1	Prolactinoma	4	Multiple endocrine neoplasia syndrome type 2A	4
				Ovotesticular disorder of sex development	1	Childhood-onset craniopharyngioma	6	Genetic obesity	4
				Partial androgen insensitivity syndrome (PAIS)	1	Septo-optical dysplasia	2	Childhood-onset osteopenia	1
				Premature ovarian failure	2			X-linked osteoporosis	2
				Klinefelter syndrome	5			Von Hippel-Lindau disease	1
				Turner syndrome	19
				Vanishing testes	2
				XXYY syndrome	1
				17-beta-HSD-deficiency	1
Total	24		20		55		38		43