Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
Autoimmune polyendocrinopathy syndrome 4 is disorder that segregates in families. Though linkage to several loci has been established no causal gene has been identified yet. Type 4 disease is characterised by two or more autoimmune disease which do not fall into type 1-3 (thyroiditis and adrenal insufficiency).
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Betterle C et al. (2002) Autoimmune adrenal insufficiency and autoimmune polyendocrine syndromes: autoantibodies, autoantigens, and their applicability in diagnosis and disease prediction. 
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| 2. |
Zirilli G et al. (2017) Peculiarities of autoimmune polyglandular syndromes in children and adolescents.
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| 3. |
Falorni A et al. (2016) From Genetic Predisposition to Molecular Mechanisms of Autoimmune Primary Adrenal Insufficiency.
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