206 top medical experts on type 1 Autoimmune polyendocrinopathy syndrome across 21 countries and 6 U.S. states, including 32 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- type 1 Autoimmune polyendocrinopathy syndrome: A rare, genetic, disease that manifests in childhood or early adolescence with a combination of chronic mucocutaneous candidiasis, hypoparathyroidism and autoimmune adrenal failure.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Synonyms: Autosomal Dominant Type I Autoimmune Polyendocrinopathy Syndrome, With Reversible Metaphyseal Dysplasia Type I Autoimmune Polyendocrinopathy Syndrome, type 1 Autoimmune polyendocrine syndrome, Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED), Hypoadrenocorticism with hypoparathyroidism and superficial moniliasis, Persian-Jewish Type Polyglandular Deficiency Syndrome
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