24 July 2008
4 A Syndrome
Sujoy Ghosh, Debmalya Sanyal, Sarmistha Mukherjee, Moutusi Raychowdhuri, Satinath Mukherjee, Subhankar ChowdhuryAm J Case Rep 2008; 9:329-332 :: ID: 865123
Abstract
Background: Allgrove syndrome is a rare inherited familial disorder with variable age of onset and presentation. It is usually diagnosed in the first decade of life with features of primary adrenal insufficiency characterized by hypoglycaemic seizures, shock and pigmentation. Less frequently, a child may be present with dysphagia due to achalasia or with ocular symptoms of dry eyes. Manifestations in adult patients are rarely reported.
Case Report: We report a case of an 18-year-old boy with undiagnosed adrenal insufficiency and neurological problems associated with deficient tear secretion (alacrima) and asymptomatic achalasia.
Conclusions: This case highlights the spectrum of abnormalities associated with Allgrove syndrome and that the diagnosis of Allgrove syndrome should be considered in all patients presenting with any one of the classic symptoms. Other features, even if asymptomatic should be explored.
Keywords: adrenal insufficiency, achalasia, alacrima, adrenal myeloneuropathy
In Press
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.949976
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.950290
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.950607
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.950985
Most Viewed Current Articles
07 Dec 2021 : Case report
17,691,734
DOI :10.12659/AJCR.934347
Am J Case Rep 2021; 22:e934347
06 Dec 2021 : Case report
164,491
DOI :10.12659/AJCR.934406
Am J Case Rep 2021; 22:e934406
21 Jun 2024 : Case report
113,090
DOI :10.12659/AJCR.944371
Am J Case Rep 2024; 25:e944371
07 Mar 2024 : Case report
59,175
DOI :10.12659/AJCR.943133
Am J Case Rep 2024; 25:e943133






