Allgrove Syndrome without esophageal achalasia: Case report
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Keywords

Acalasia del esófago
Insuficiencia suprarrenal
Alacrimia
Síndrome de Allgrove
Reporte de caso Esophageal Achalasia
Adrenal Insufficiency
Lacrimal Apparatus Diseases
Allgrove Syndrome
Case report

How to Cite

Quintero-Palacios, M. A. . ., Nofal-Ladino, J. J. ., Roa-Rodríguez, S. M. ., & Palacios-Ariza, M. A. . (2022). Allgrove Syndrome without esophageal achalasia: Case report. Revista Médica Sanitas, 25(1), 7-14. https://doi.org/10.26852/01234250.612

Abstract

Allgrove Syndrome is an orphan disease with an autosomal recessive inheritance pattern distinguished by the triad of suprarenal insufficiency, achalasia and alacrimia. We describe the case of a previously healthy male preschooler who was admitted to the emergency department of a tertiary care center in poor general status. The patient completed a 25-day hospital stay in which he presented multiple cardiorespiratory arrests, aspiration pneumonia, symptomatic hypoglycemia and a poor response to corticosteroids which gave rise to a suspicion of a metabolic disease. In the outpatient pediatric endocrinology clinic, additional features were noted: generalized skin hyperchromia, alacrimia, and inadequate weight and height gain in the absence of gastroesophageal reflux or achalasia. Allgrove syndrome is an illness with a broad spectrum of manifestations which should be considered despite the absence of the usual triad.

https://doi.org/10.26852/01234250.612
PDF (Español (España))

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