"T2: lower signal intensity than surrounding atrophic adrenal tissue ref"
Expected headings
"Associations"
"PPNAD is often familial. Patients typically present in childhood or young adulthood, with a median age of diagnosis being 34 years 1,4. There is a female predilection of 2:1 1,3."
"Multiple gene mutations have been implicated; the most common is a mutation in the PRKAR1A gene (~80%), which is inherited in an autosomal dominant pattern 2,3."