Allgrove Syndrome: A Case Report
| Author | A Soltani | en |
| Author | M Arab Ameri | en |
| Author | SH Hasani Ranjbar | en |
| Issued Date | 2007-10-31 | en |
| 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. | en |
| DOI | https://doi.org/ | en |
| Keyword | Allgrove syndrome | en |
| Keyword | Achalasia | en |
| Keyword | Alacrima | en |
| Keyword | Addison | en |
| Keyword | Adrenocorticotropin insensitivity syndrome. | en |
| Publisher | Brieflands | en |
| Title | Allgrove Syndrome: A Case Report | en |
| Type | Case Report | en |
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