@Article{Hogendorf2016,
journal="Pediatric Endocrinology Diabetes and Metabolism",
issn="2081-237X",
volume="22",
number="2",
year="2016",
title="Alkaptonuria in a boy with type 1 diabetes mellitus, vitiligo, autoimmune thyroiditis and immunoglobulin A deficiency – a case report",
abstract="We present a 15-year-old Caucasian boy with an exceptional coincidence of a rare monogenic metabolic disease – alkaptonuria (AKU) and a cluster of  autoimmune disorders: type 1 diabetes (T1DM), autoimmune thyroiditis (AIT), vitiligo, insulin infusion induced lipoatrophy and immunoglobulin A deficiency (IgAD) Alkaptonuria and type 1 diabetes in a child, especially in such an interesting coincidence with other autoimmune conditions, has not been reported so far. Our investigation, including comprehensive genetic evaluation using next generation sequencing technology, shows that alkaptonuria and T1DM were independently inherited. We also show that alkaptonuria in its pre-ochronotic phase seems to have no effect on the course of diabetes.",
author="Hogendorf, Anna
and Pietrzak, Iwona
and Antosik, Karolina
and Borowiec, Maciej
and Młynarski, Wojciech",
url="https://www.termedia.pl/-Alkaptonuria-u-chlopca-z-cukrzyca-typu-1-bielactwem-autoimmunologicznym-zapaleniem-tarczycy-i-niedoborem-immunoglobuliny-A-,138,36594,1,1.html"
}