Clinical and genetic analysis of a case of Gitelman syndrome with comorbid Graves disease and adrenocortical adenoma.
10.3760/cma.j.cn511374-20210922-00767
- Author:
Yan QIAO
1
;
Jinghong ZHAO
;
Lewei CAO
;
Yunxiang LI
;
Ji WU
Author Information
1. Department of Endocrinology, Nanchong Central Hospital, Nanchong, Sichuan 637003, China. 604186116@qq.com.
- Publication Type:Journal Article
- MeSH:
Humans;
Female;
Middle Aged;
Gitelman Syndrome/genetics*;
Adrenocortical Adenoma;
Hypokalemia;
Graves Disease/genetics*;
Mothers;
Mutation;
Solute Carrier Family 12, Member 3
- From:
Chinese Journal of Medical Genetics
2023;40(11):1409-1413
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To report the clinical and genetic characteristics of a rare case of Gitelman syndrome with comorbid Graves disease and ACTH-independent adrenocortical adenoma.
METHODS:A patient who had presented at the Nanchong Central Hospital on December 21, 2020 was selected as the study subject. Clinical data of the patient was collected. Whole-exome sequencing was carried out on DNA extracted from peripheral venous blood samples from the patient and her family members.
RESULTS:The patient, a 45-year-old woman, was found to have Graves disease, ACTH-independent Cushing syndrome, hypokalemia and hypomagnesemia following the discovery of an adrenal incidentaloma. MRI scan had revealed a 3.8 cm × 3.2 cm mass in the left adrenal gland. The mass was removed by surgery and confirmed as adrenocortical adenoma. DNA sequencing revealed that the patient and her sister have both harbored compound heterozygous variants of the SLC12A3 gene, namely c.1444-10(IVS11)G>A and c.179(exon1)C>T (p.T60M), which were respectively inherited from their father and mother. Based on the guidelines from the American College of Medical Genetics and Genomics (ACMG), the c.1444-10(IVS11)G>A and c.179(exon1)C>T (p.T60M) were respectively classified as a variant of uncertain significance (PM2_Supporting+PP3) and a likely pathogenic variant (PM3_Strong+PM1+PP3).
CONCLUSION:The conjunction of Gitelman syndrome with Graves disease and adrenal cortex adenoma is rather rare. The newly discovered c.1444-10(IVS11)G>A variant of the SLC12A3 gene, together with the heterozygous variant of c.179(exon1)C>T (p.T60M), probably underlay the pathogenesis in this patient.
