Allgrove syndrome with amyotrophy

Abstract

Allgrove syndrome is an autosomal recessive disease mostly caused by mutations in the AAAS gene. It has variable clinical features but its cardinal features comprise the triad of achalasia, alacrimia and adrenal insufficiency. It typically develops during the first decade of life, but some cases have second and third decades onset. We describe a 25-year-old woman with Allgrove syndrome who had progressive amyotrophy, achalasia, dry eyes and adrenal insufficiency since childhood. Awareness of its neurological manifestations and multisystem features helps to shorten the time for diagnosis and allow appropriate symptomatic treatment.

Síndrome de Allgrove e amiotrofia: uma associação rara

“…Também conhecida como Síndrome do Triplo A, é caracterizada por uma tríade clássica: acalasia, alacrimia e insuficiência adrenal primária (IA), sendo esta devido à resistência ao hormônio adrenocorticotrófico (JAYANT et al, 2021;SOARES et al, 2022).…”