Meloni et al., "Cytochrome P450 1A2 Is a Hepatic Autoantigen in Autoimmune Polyglandular
Syndrome Type 1 ," The Journal of Clinical Endocrinology & Metabolism, vol.
Type 1 diabetes and autoimmune polyglandular
syndrome: a critical review.
She might have a polyglandular
deficiency due to her diagnosis of Graves' hyperthyroidism and diabetes mellitus, i.e.
autoimmune syndromes: immunogenetics and long-term follow-up.
For instance, the company's steroid 21-hydroxylase antibody (21-0HAb) test kit may be useful as an aid in the diagnosis of autoimmune adrenal disease, whether expressed as autoimmune Addison's Disease or Addison's Disease as part of the more complex autoimmune polyglandular
syndrome (APS), Type I or II.
Other diseases of connection to Sephardi origin include: Alpha-Thalassemia, Ataxia Telangiectasia, Corticosterone Methyloxidase Type II Deficiency, Costeff Optical Atrophy, Cystic Fibrosis (CF), Familial Creutzfeldt-Jakob Disease, Familial Tumoral Calcinosis (Normophosphatemic Type), Inclusion Body Myophy Type 28, Metachromic Leukodystrophy, Polyglandular
Deficiency Syndrome, Pseudocholinesterase Deficiency, Spinal Muscular Athrophy (S.MA) and Wolman Disease.
Premature ovarian failure associated with autoimmune polyglandular
syndrome: pathophysiological mechanism and future fertility.
In general, hypothyroidism discovered before the age of three is considered to represent a failure of newborn screening, though cases associated with a rare disease of the endocrine system called polyglandular
autoimmune syndrome have been reported.