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Genetic diagnosis on one case of primary pigmented nodular adrenal disease / 中华内分泌代谢杂志
Chinese Journal of Endocrinology and Metabolism ; (12): 231-233, 2011.
Article in Chinese | WPRIM | ID: wpr-413821
ABSTRACT
Primary pigmented nodular adrenal disease (PPNAD) is a kind of autosomal dominant inherited disease. Patient in the study presented with Cushing's syndrome, and clinical and pathological diagnosis of PPNAD was confirmed. It is now confirmed that there are two relevant genes and their mutations may lead to PPNAD. This study showed no mutations in the patient, surpecting if there would be an alternative mechanism or a new gene in playing the role.

Full text: Available Index: WPRIM (Western Pacific) Type of study: Diagnostic study Language: Chinese Journal: Chinese Journal of Endocrinology and Metabolism Year: 2011 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Type of study: Diagnostic study Language: Chinese Journal: Chinese Journal of Endocrinology and Metabolism Year: 2011 Type: Article