若光云医学:第三节 胎儿脑积水(18-3)
其相关疾病及致病基因、表型等简述如下表18-5:
氨基蝶呤综合征参见第四十章母源代谢性先天畸形;线粒体复合体IV缺乏症参见线粒体病相关内容。
其他还有多种已有报告具有脑积水表型未明确致病基因的相关疾病,以及动物实验研究发现的脑积水相关致病基因,本节不再赘述。
(王若光)
参考文献
[16] Rehnberg M, JonassonJ, Gunnarsson C. Novel L1CAM splice site mutation in a young male with L1syndrome[J]. (Letter) Am. J. Med. Genet. 155: 439-441, 2011.
[17] Drielsma A, Jalas C,Simonis N, et al. Two novel CCDC88C mutations confirm the role of DAPLE inautosomal recessive congenital hydrocephalus[J]. J. Med. Genet. 49: 708-712,2012.
[18] Shaheen R, Sebai M A, Patel N, et al. The geneticlandscape of familial congenital hydrocephalus[J]. Ann. Neurol. 81: 890-897,2017.
[19] Nakamura K, Kato M, Tohyama J, et al. AKT3 and PIK3R2mutations in two patients with megalencephaly-related syndromes: MCAP andMPPH[J]. (Letter) Clin. Genet. 85: 396-298, 2014.
[20] Cho G, Nasrallah M P, Lim Y, et al. Distinct DNA bindingand transcriptional repression characteristics related to different ARXmutations[J]. Neurogenetics 13: 23-29, 2012.