A pedigree study of a patient with primary pigmented nodular adrenocortical disease and familial gene mutation
10.3760/cma.j.issn.0578-1426.2014.05.015
- VernacularTitle:原发性色素性结节样肾上腺皮质病一例及其家系的基因突变研究
- Author:
Hui RAN
;
Xiaokun MA
;
Qingzhu WANG
;
Ziyi XIE
;
Yanxia DING
;
Guijun QIN
- Publication Type:Journal Article
- Keywords:
Cushing syndrome;
Primary pigmented nodular adrenocortical disease;
Mutation;
PRKAR1A
- From:
Chinese Journal of Internal Medicine
2014;53(5):398-402
- CountryChina
- Language:Chinese
-
Abstract:
Objective To clarify the clinical features and genetic background of a kindred of primary pigmented nodular adrenocortical disease (PPNAD).Methods Detailed clinical characteristics and laboratory test results from a ten-year old girl diagnosed as PPNAD were collected.Seven members of her family were screened for Cushing syndrome and Carney complex,and their blood DNA was extracted and sequenced for PRKAR1A,PDE11A,PDE8B and CTNNB1 mutations with ABI3730.Results The girl presented with symptoms and signs of hypercortisolism,while no features of Carney complex were observed.Hypercortisolemia,suppressed corticotrophin and high urinary free cortisol level were revealed.Cortisol level could not be suppressed both in high and low dose dexamethasone suppression test.The diagnosis of adrenocorticotrophic hormone (ACTH)-independent Cushing syndrome was established.Image and pathology of adrenal glands were in accordance with PPNAD.Other family members showed no evidence of Cushing syndrome or Carney complex.DNA sequencing showed that the patient harbored a missense mutation,C18G.Her father and younger sister were proved to be carriers of this mutation.Conclusion A Chinese PPNAD family was identified clinically and genetically,and a novel missense mutation of PRKAR1A was found.
