ea0056p94 | Clinical case reports - Pituitary/Adrenal | ECE2018
Petrescu Denisa
, Silaghi Cristina Alina
, Albu Adriana
, Silaghi Horatiu
, Lungu Ionela
, Suciu-Petrescu Malina
, Bucerzan Simona
, Georgescu Carmen Emanuela
Autoimmune Polyglandular Syndrome Type I (APS 1) is a rare monogenic disease, in which simultaneous or sequential dysfunctions of endocrine or nonendocrine glands appear. A 19-year-old woman was admitted for inappetence, nausea, vomiting, abdominal pain, chronic constipation, generalized paresthesia and vertigo. She was known with primary hypoparathyroidism (from the age of 5), chronic autoimmune thyroiditis, mucocutaneous candidiasis, under treatment with calcitriol, calcium,...