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International Journal of Endocrinology and Metabolism
Research Institute for Endocrine Sciences
Allgrove Syndrome: A Case Report
Author(s):
1Endocrinology and Metabolism Research Center, Tehran University of Medical Sciences, [email protected], I.R Iran
2Endocrinology and Metabolism Research Center, Tehran University of Medical Sciences, I.R Iran
*Corresponding Author: Endocrinology and Metabolism Research Center, Tehran University of Medical Sciences, [email protected], I.R Iran. Email: [email protected]
Published online:Oct 31, 2007
Article type:Case Report
Received:Jun 09, 2007
Accepted:Jul 17, 2007
How to Cite:Soltani A, Arab Ameri M, Hasani Ranjbar S. Allgrove Syndrome: A Case Report. Int J Endocrinol Metab. 2007;5(4):. doi:
Abstract
Allgrove syndrome (triple A syndrome) is an autosomal recessive disorder characterized by achalasia, alacrima and adrenocorticotropic hor-mone (ACTH) resistant adrenal insufficiency. It is a multisystem disease and in addition to cardinal manifestations, associated features es-pecially neurologic problems, must be detected and treated. In this case report, we report a 17 year-old boy diagnosed as having Allgrove syndrome with predominant symptoms of achalasia and additional features consisting of short neck, long eye lashes, unexplained fever and chills, reduced visual acuity because of amblyopia, thenar and hypothenar atrophy and abnormal opposition of fingers. If necessary screening with stimulatory tests in patients with unexplained features such as long eye lashes, short neck, muscle atrophy, na-sal speech, skin and neurologic abnormalities and hyperkeratosis, should be recommended.
Copyright
© 2007, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.
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