This is a case report of 2 patients who were diagnosed to have autoimmune p
olyglandular disease type 1. Both developed mucocutaneous candidiasis, hypo
parathyroidism, vitiligo, and adrenocortical insufficiency. Both were notic
ed to have subnormal linear growth velocity and delayed bone age. Both show
ed subnormal stimulated serum growth hormone values indicating growth hormo
ne deficiency. The first case showed favorable response to growth hormone t
herapy.