Browsing by Subject "4A SYNDROME"

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A broad range of symptoms in allgrove syndrome: single center experience in Southeast Anatolia

Polat, R.; Ustyol, A.; Tuncez, E.; Guran, T. (SPRINGER, 2020)

Background Allgrove syndrome (OMIM 231550) is a rare autosomal recessive disease characterized by non-CAH primary adrenal insufficiency (non-CAH PAI), alacrima, and achalasia. It is caused by mutations in the AAAS gene. ...