SAT-242 Pigmented Paravenous Retinochorodial Atrophy: A Novel Manifestation of Autoimmune Polyglandular Syndrome Type 1

Autoimmune polyglandular Syndrome Type 1 (APS-1) is an autoimmune disease due to defects in the AIRE gene. It is characterized by a triad of hypoparathyroidism, mucocutaneous candidiasis, and Addison’s disease. We present a case of pigmented paravenous retinochoroidal atrophy associated with APS-1....

Descripción completa

Detalles Bibliográficos
Autores principales: Zachary, Tyler, Garla, Vishnu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2019
Materias:
Pediatric Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6551724/
http://dx.doi.org/10.1210/js.2019-SAT-242

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6551724/
http://dx.doi.org/10.1210/js.2019-SAT-242

Ejemplares similares