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Allgrove syndrome: a case report

Allgrove syndrome (AS), or Triple-A syndrome, is a multi-system disorder characterized by alacrima (a decrease or absence of tear production), adrenal insufficiency and achalasia (absence of esophageal muscle peristalsis and failure to relax the lower esophageal sphincter). This syndrome may affect...

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Autores principales: Alhalabi, Marouf, Alsayd, Saddam, Alboushi, Ebtesam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9589468/
https://www.ncbi.nlm.nih.gov/pubmed/36299673
http://dx.doi.org/10.1093/omcr/omac104
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author Alhalabi, Marouf
Alsayd, Saddam
Alboushi, Ebtesam
author_facet Alhalabi, Marouf
Alsayd, Saddam
Alboushi, Ebtesam
author_sort Alhalabi, Marouf
collection PubMed
description Allgrove syndrome (AS), or Triple-A syndrome, is a multi-system disorder characterized by alacrima (a decrease or absence of tear production), adrenal insufficiency and achalasia (absence of esophageal muscle peristalsis and failure to relax the lower esophageal sphincter). This syndrome may affect the autonomic nervous system, in which case it is called a 4A syndrome. It is a rare autosomal recessive inheritance, and early identification is difficult due to the rarity and wide phenotypic variation even among members of the same family. Endocrinologists, gastroenterologists, ophthalmologists, neurologists and surgeons are needed to coordinate care for these patients. We describe a case of AS that took several years to complete the diagnosis. She was diagnosed with alacrima at the age of 1-year-old, adrenal insufficiency at the age of 9 and achalasia at the age of 16. This case demonstrates the difficulty and delay in the diagnosis of AS.
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spelling pubmed-95894682022-10-25 Allgrove syndrome: a case report Alhalabi, Marouf Alsayd, Saddam Alboushi, Ebtesam Oxf Med Case Reports Case Report Allgrove syndrome (AS), or Triple-A syndrome, is a multi-system disorder characterized by alacrima (a decrease or absence of tear production), adrenal insufficiency and achalasia (absence of esophageal muscle peristalsis and failure to relax the lower esophageal sphincter). This syndrome may affect the autonomic nervous system, in which case it is called a 4A syndrome. It is a rare autosomal recessive inheritance, and early identification is difficult due to the rarity and wide phenotypic variation even among members of the same family. Endocrinologists, gastroenterologists, ophthalmologists, neurologists and surgeons are needed to coordinate care for these patients. We describe a case of AS that took several years to complete the diagnosis. She was diagnosed with alacrima at the age of 1-year-old, adrenal insufficiency at the age of 9 and achalasia at the age of 16. This case demonstrates the difficulty and delay in the diagnosis of AS. Oxford University Press 2022-10-22 /pmc/articles/PMC9589468/ /pubmed/36299673 http://dx.doi.org/10.1093/omcr/omac104 Text en © The Author(s) 2022. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Case Report
Alhalabi, Marouf
Alsayd, Saddam
Alboushi, Ebtesam
Allgrove syndrome: a case report
title Allgrove syndrome: a case report
title_full Allgrove syndrome: a case report
title_fullStr Allgrove syndrome: a case report
title_full_unstemmed Allgrove syndrome: a case report
title_short Allgrove syndrome: a case report
title_sort allgrove syndrome: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9589468/
https://www.ncbi.nlm.nih.gov/pubmed/36299673
http://dx.doi.org/10.1093/omcr/omac104
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