Institute of Neurology, University Magna Græcia, Catanzaro, Italy.
Epilepsy Res. 2013 May;104(3):280-4. doi: 10.1016/j.eplepsyres.2012.10.014. Epub 2013 Jan 23.
Mutations of PRRT2, which encodes proline-rich transmembrane protein 2, are associated with heterogeneous phenotypes including benign familial infantile seizures (BFIS) and/or familial paroxysmal kinesigenic dystonia (PKD). Here, we performed mutation screening of PRRT2 in six Italian families with BFIS/PKD phenotypes. The mutation, c.649dupC (p.Arg217ProfsX8), was found in two families with BFIS phenotype. In a third BFIS family, a missense mutation, c.718C/T (R240X), was identified. All these mutations co-segregated with the disease and were not observed in 100 controls of matched ancestry. In one BFIS family that carried the c.649dupC mutation, one affected member developed afebrile focal seizures and died at age of 14 years of probable sudden unexpected death in epilepsy, while his brother also had simple febrile convulsions (FC) and performed poorly on complex psychomotor functioning. In another family carrying the c.718C/T mutation, two of three affected members also had simple FC. This study enlarges the clinical spectrum related to PPRT2 mutations and underscores the complexity of the phenotypic consequences of mutations in this gene.
PRRT2 基因编码富含脯氨酸的跨膜蛋白 2,其突变与包括良性家族性婴儿癫痫(BFIS)和/或家族性阵发性运动源性舞蹈手足徐动症(PKD)在内的异质性表型相关。在此,我们对 6 个具有 BFIS/PKD 表型的意大利家族进行了 PRRT2 基因突变筛查。在两个具有 BFIS 表型的家族中发现了突变 c.649dupC(p.Arg217ProfsX8)。在第三个 BFIS 家族中,发现了错义突变 c.718C/T(R240X)。所有这些突变与疾病共分离,在 100 名匹配种族的对照中未观察到。在携带 c.649dupC 突变的一个 BFIS 家族中,一个受影响的成员发生了无热局灶性癫痫发作,并在 14 岁时死于可能的癫痫性猝死,而他的兄弟也有单纯性热性惊厥(FC),且复杂运动心理功能表现不佳。在携带 c.718C/T 突变的另一个家族中,三个受影响成员中的两个也有单纯性 FC。本研究扩大了与 PRRT2 突变相关的临床谱,并强调了该基因突变对表型后果的复杂性。