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Allgrove syndrome

Date

2012

Author

Kilicli, Fatih
Acibucu, Fettah
Senel, Soner
Dokmetas, Hatice Sebila

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Abstract

Allgrove syndrome is a rare autosomal recessive disorder. It is also known as the 3A syndrome and characterised by the triad of achalasia, alacrima and adrenal insufficiency. The AAAS gene is encoded on chromosome 12q13. We report the case of a 23-year-old woman who presented at the hospital with adrenal crisis that was triggered by infection of the urinary system and gastrointestinal bleeding. She had a known diagnosis of achalasia for eight years, and ophthalmologic examination revealed alacrima. Based on our findings, the patient was diagnosed with Allgrove syndrome.

Source

SINGAPORE MEDICAL JOURNAL

Volume

53

Issue

5

URI

https://hdl.handle.net/20.500.12418/9141

Collections

  • Makale Koleksiyonu [5200]
  • Makale Koleksiyonu [5745]
  • Öksüz Yayınlar Koleksiyonu - WoS [6162]



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