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Triple A syndrome.
Bharadia, Lalit; Kalla, Mukesh; Sharma, S K; Charan, Rohit; Gupta, J B; Khan, Firoz.
Article in English | IMSEAR | ID: sea-65310

ABSTRACT

Triple A syndrome (Allgrove syndrome) is an autosomal recessive disorder consisting of achalasia, alacrima and Addison insufficiency. We report an 11-year-old girl with predominant symptom of achalasia who was diagnosed as Triple A syndrome almost 3 years after initial presentation.


Subject(s)
Addison Disease/diagnosis , Child , Esophageal Achalasia/diagnosis , Female , Humans , Lacrimal Apparatus Diseases/diagnosis , Mutation , Nerve Tissue Proteins , Nuclear Pore Complex Proteins , Proteins/genetics , Syndrome
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