September 27, 2005European Journal of Endocrinology
Molecular genetics of adrenocortical tumours, from familial to sporadic diseases
Population
Patients with adrenocortical tumours, including familial syndromes and sporadic diseases
Design
Review
Authors
Discussion
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Implication
This review highlights the critical role of molecular genetics in understanding the pathogenesis and improving the diagnosis of both familial and sporadic adrenocortical tumours.
Structured PICO
P
Population
Patients with adrenocortical tumours (ACTs), including familial syndromes (Li-Fraumeni, Beckwith-Wiedemann, MEN 1, Carney complex) and sporadic diseases
This review highlights the critical role of molecular genetics in understanding the pathogenesis and improving the diagnosis of both familial and sporadic adrenocortical tumours.
Cite This Study
Libé et al. (2005) studied this question.