Literature DB >> 33070704

Triple A syndrome: a case report.

Piyush Manoria1.   

Abstract

Triple A syndrome is a rare autosomal recessive disorder characterised by alacrimia, achalasia and adrenal failure. It was first reported by Allgrove in 1978 and 100 cases have been reported worldwide. This case report concerns a 24-year-old woman who was referred for evaluation of dysphagia and was finally diagnosed as such a case. A high degree of suspicion enables all the components of this syndrome to be searched for, as early diagnosis can reduce the morbidity and mortality.

Entities:  

Keywords:  Alacrimia; achalasia; adrenal insufficiency

Mesh:

Year:  2020        PMID: 33070704     DOI: 10.1177/0049475520961944

Source DB:  PubMed          Journal:  Trop Doct        ISSN: 0049-4755            Impact factor:   0.731


  1 in total

1.  Mineralocorticoid Deficiency as an Early Presenting Symptom of Allgrove Syndrome With Novel Mutation: A Case Report.

Authors:  Hashem A AlOmran; Fadi Busaleh; Zahra Alhashim; Manal AlHelal; Yasen Alsaleh; Aida AlJabri; Zahra A AlGhadeer; Fatimah Y AlHejji; Mousa AlMazeedi; Abdulelah M Al Dandan
Journal:  Cureus       Date:  2021-11-06
  1 in total

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