Child Neurology Unit, Hospital Universitario 12 de Octubre, Carretera de Andalucía km 5,4, 28041 Madrid, Spain.
Epilepsy Behav. 2012 May;24(1):134-7. doi: 10.1016/j.yebeh.2012.02.023. Epub 2012 Apr 14.
Mutation in the protocadherin 19 (PCDH19) gene is an increasingly recognized cause of epilepsy in females. This disorder is frequently associated with mental retardation and psychiatric features. We describe two unrelated females with novel PCDH19 missense mutations. One was de novo, and the other was inherited from her unaffected father. Both had mild mental impairment but had remarkable behavioral problems. We reviewed the cognitive and behavioral profiles of previously reported PCDH19-positive cases. Intellectual disability appeared in 75% of patients, ranging from borderline to severe. More than half of the individuals presented behavioral disturbances, which could be divided into two different groups: autistic and non-autistic. The majority of patients with autism already had some degree of cognitive impairment. It appears that seizures tend to diminish or even stop in adolescence, so non-epileptic problems can become the most important and disabling issue in adult patients with PCDH19 mutation.
原钙黏蛋白 19 (PCDH19)基因突变是女性癫痫越来越被认可的病因。该疾病常伴有智力迟钝和精神症状。我们描述了 2 例无关联的女性,均存在新的 PCDH19 错义突变。1 例为新生突变,另 1 例源自未患病父亲。2 例均有轻度智力障碍,但均有明显的行为问题。我们复习了既往报道的 PCDH19 阳性病例的认知和行为特征。75%的患者存在不同程度的智力障碍,从边缘智力到重度。超过一半的个体存在行为障碍,可分为两类:自闭症和非自闭症。大多数自闭症患者已经有一定程度的认知障碍。癫痫发作似乎在青春期减少甚至停止,因此非癫痫性问题可能成为 PCDH19 突变成年患者最重要和致残的问题。