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Article

[Allgrove syndrome. Report on a family].

Journal francais d'ophtalmologie - 1 Apr 2006

Sellami D, Bouacida W, Frikha F, Triki C, BenZina Z, Ben Salah S, Feki J, Sellami A

Abstract excerpt

Triple A or Allgrove syndrome is a rare autosomal recessive disease with alacrima, achalasia, and ACTH-resistant adrenal insufficiency. It is usually associated with neurological disorders. Recently, mutations in the AAAS, a candidate gene mapped to chromosome 12q13, were identified. We report a family with seven affected siblings. All of them have signs of alacrima, four were operated on for achalasia, five have...

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Identifiers

PMID: 16885810
DOI: 10.1016/s0181-5512(06)77702-6

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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