Copyright
©The Author(s) 2022.
World J Clin Cases. Mar 26, 2022; 10(9): 2844-2850
Published online Mar 26, 2022. doi: 10.12998/wjcc.v10.i9.2844
Published online Mar 26, 2022. doi: 10.12998/wjcc.v10.i9.2844
Figure 1 Genetic research of the family.
A: Patient’s family tree; B: Genetic analysis of SLC12A3 in patient’s family. a1 and b1: Father, a carrier of GS-associated mutations, SLC12A3: c.179C>T in exon1; a2 and b2: Mother, a carrier of GS-associated mutations, c.965-1_976 delins ACCGAAAATTTT in exon8; a3 and b3: The eldest daughter; a4 and b4: The third eldest daughter; a5 and b5: Index patient; a3-a5 and b3-b5: Revealed compound heterozygous mutations of the gene SLC12A3: c.179C>T in exon1 and c.965-1_976delinsACCGAAAATTTT in exon8; b6: Gene analysis of Wild type.
- Citation: Wu CY, Tsai MH, Chen CC, Kao CH. Early diagnosis of Gitelman syndrome in a young child: A case report . World J Clin Cases 2022; 10(9): 2844-2850
- URL: https://www.wjgnet.com/2307-8960/full/v10/i9/2844.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v10.i9.2844