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Triple A (Allgrove) syndrome due to AAAS gene mutation with a rare association of amyotrophy.

Satyam Singh JayantRahul GuptaKanhaiya AgrawalLiza DasPinaki DuttaAnil Bhansali
Published in: Hormones (Athens, Greece) (2020)
In any young patient with AI not due to congenital adrenal hyperplasia, Allgrove syndrome should be ruled out. Though mineralocorticoid sparing pattern is classical, it can rarely be involved, as seen in the index case. Various components of the syndrome, as well as amyotrophy and other neurologic features, may present in a metachronous fashion. Hence, a high index of clinical suspicion can aid in early diagnosis and management.
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