已经报告具神经管缺陷表型,致病基因未明确的疾病:同卵双生及结构畸形,颈-眼-耳综合征,高同型半胱氨酸血症,细胞叶酸水平,颅面畸形白内障先天性心脏病骶骨神经型管缺陷以及生长发育迟缓症,Poland综合征,Fryns小眼综合征,眼-耳-脊椎畸形谱,胃裂-腹壁缺陷等。
(王陆颖,王若光)
参考文献
[33]李宏智.神经管畸形病因遗传学研究进展[J].临床军医杂志,46(6):-.
[34]王蕾,王珊,裴培,等.神经管畸形的表观遗传学研究进展[J].现代生物医学进展,18(6):-.
[35]LoganCV,Abdel-HamedZ,JohnsonCA.Moleculargeneticsandpathogenicmechanismsforthesevereciliopathies:insightsintoneurodevelopmentandpathogenesisofneuraltubedefects[J].Molec.Neurobiol.,43:12-26.
[36]RobinsonA,EscuinS,DoudneyK,etal.MutationsintheplanarcellpolaritygenesCELSR1andSCRIBareassociatedwiththesevereneuraltubedefectcraniorachischisis[J].Hum.Mutat.,33:-.
[37]DetraitER,GeorgeTM,EtcheversHC,etal.Humanneuraltubedefects:developmentalbiology,epidemiology,andgenetics[J].Neurotoxicol.Teratol.,27:-.
[38]AbeY,MatsudukaA,OkanariK,etal.Aseverepulmonary