Article
A Longitudinal Follow-up of Autoimmune Polyendocrine Syndrome Type 1.
The Journal of clinical endocrinology and metabolism - 1 Aug 2016
Bruserud Øyvind, Oftedal Bergithe E, Landegren Nils, Erichsen Martina M, Bratland Eirik, Lima Kari, Jørgensen Anders P, Myhre Anne G, Svartberg Johan, Fougner Kristian J, Bakke Åsne, Nedrebø Bjørn G, Mella Bjarne, Breivik Lars, Viken Marte K, Knappskog Per M, Marthinussen Mihaela C, Løvås Kristian, Kämpe Olle, Wolff Anette B, Husebye Eystein S
Abstract excerpt
CONTEXT: Autoimmune polyendocrine syndrome type 1 (APS1) is a childhood-onset monogenic disease defined by the presence of two of the three major components: hypoparathyroidism, primary adrenocortical insufficiency, and chronic mucocutaneous candidiasis (CMC). Information on longitudinal follow-up of APS1 is sparse. OBJECTIVE: To describe the phenotypes of APS1 and correlate the clinical features with...
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