Triple A syndrome.

Bharadia, Lalit; Kalla, Mukesh; Sharma, S K; Charan, Rohit; Gupta, J B; Khan, Firoz

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

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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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Syndrome / Female / Humans / Addison Disease / Proteins / Esophageal Achalasia / Child / Nuclear Pore Complex Proteins / Lacrimal Apparatus Diseases / Mutation Language: English Year: 2005 Type: Article

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