Brownstein Catherine A, Towne Meghan C, Luquette Lovelace J, Harris David J, Marinakis Nicholas S, Meinecke Peter, Kutsche Kerstin, Campeau Philippe M, Yu Timothy W, Margulies David M, Agrawal Pankaj B, Beggs Alan H
Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Eur J Med Genet. 2013 Dec;56(12):678-82. doi: 10.1016/j.ejmg.2013.09.009. Epub 2013 Oct 28.
KCNJ8 (NM_004982) encodes the pore forming subunit of one of the ATP-sensitive inwardly rectifying potassium (KATP) channels. KCNJ8 sequence variations are traditionally associated with J-wave syndromes, involving ventricular fibrillation and sudden cardiac death. Recently, the KATP gene ABCC9 (SUR2, NM_020297) has been associated with the multi-organ disorder Cantú syndrome or hypertrichotic osteochondrodysplasia (MIM 239850) (hypertrichosis, macrosomia, osteochondrodysplasia, and cardiomegaly). Here, we report on a patient with a de novo nonsynonymous KCNJ8 SNV (p.V65M) and Cantú syndrome, who tested negative for mutations in ABCC9. The genotype and multi-organ abnormalities of this patient are reviewed. A careful screening of the KATP genes should be performed in all individuals diagnosed with Cantú syndrome and no mutation in ABCC9.
KCNJ8(NM_004982)编码一种ATP敏感性内向整流钾通道(KATP)的孔形成亚基。传统上,KCNJ8序列变异与J波综合征有关,涉及心室颤动和心源性猝死。最近,KATP基因ABCC9(SUR2,NM_020297)已与多器官疾病坎图综合征或多毛性骨软骨发育不良(MIM 239850)(多毛症、巨体症、骨软骨发育不良和心脏肥大)相关。在此,我们报告1例患有新发非同义KCNJ8单核苷酸变异(p.V65M)和坎图综合征的患者,其ABCC9基因突变检测为阴性。对该患者的基因型和多器官异常情况进行了回顾。对于所有诊断为坎图综合征且ABCC9无突变的个体,应仔细筛查KATP基因。