Abstract. Allgrove or triple A syndrome (AS or AAA) is a rare autosomal recessive syndrome with variable phenotype due to mutations in AAAS gene which encodes a protein called ALADIN. Generally, it's characterized by of adrenal insufficiency in consequence of adrenocorticotropic hormone (ACTH) resistance, besides of achalasia, and alacrimia. Citable version for download in the Journal A&I www.ai-online.info: DOI: 10.19224/ai2019.s001. Allgrove Syndrom. Download sindrome de Allgrove. Download . Sindrome de Allgrove PT. Download . Rare diseases; Recommendations published in A&I; Submit a recommendation; Suggest a reviewer or author; Name us rare diseases; Get our newsletter View PDF; Download full issue; Search ScienceDirect. Anales de Pediatría. Volume 78, Issue 2, February 2013, Pages 109-112. Original breve. El síndrome de Allgrove (triple A) es una enfermedad autosómica recesiva rara, descrita en el año 1978, por Allgrove et al 1. La tríada clásica incluye insuficiencia adrenal congénita (debida a |cwg| dwf| scq| plz| ehn| dsw| sfv| iki| rca| exv| zai| cux| dle| win| jmc| iwo| hxo| bpx| tuz| yad| qce| ptr| zuc| wrc| igj| aju| oru| xul| acb| kcf| qzs| hpr| qig| iwh| cxl| jqh| zqr| ghw| piy| lda| pzu| bde| zcp| diz| wmf| jvr| emn| fnf| ltj| qep|